Abstract
Common variable immunodeficiency (CVID) is the most prevalent symptomatic primary immune deficiency. With widespread use of immunoglobulin replacement therapy, non-infectious complications, such as autoimmunity, chronic intestinal inflammation, and lung disease, have replaced infections as the major cause of morbidity and mortality in this immune deficiency. The pathogenic mechanisms that underlie the development of these complications in CVID are not known; however, there have been numerous associated laboratory findings. Among the most intriguing of these associations is elevation of interferon signature genes in CVID patients with inflammatory/autoimmune complications, as a similar gene expression profile is found in systemic lupus erythematosus and other chronic inflammatory diseases. Linked with this heightened interferon signature in CVID is an expansion of circulating IFN-γ-producing innate lymphoid cells. Innate lymphoid cells are key regulators of both protective and pathogenic immune responses that have been extensively studied in recent years. Further exploration of innate lymphoid cell biology in CVID may uncover key mechanisms underlying the development of inflammatory complications in these patients and may inspire much needed novel therapeutic approaches.
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Introduction
Common variable immunodeficiency (CVID) is the most common symptomatic primary immune deficiency with an incidence estimated at 1:25,000, though this can vary in different locations [1, 2]. Importantly, CVID is a heterogeneous disorder of diverse genetic etiologies all leading to a shared phenotype of profound antibody deficiency [3]. While the genetic causes of CVID are known for only a minority of patients, the list of mutations associated with this immune deficiency has been steadily increasing through extensive research efforts [4, 5]. To meet the diagnostic criteria of CVID, patients must have marked reductions of serum IgG, IgA, and/or IgM (conventionally at least two standard deviations below reference levels) along with impaired antibody responses to vaccination, often with extensive reduction of isotype-switched memory B cells [6]. CVID patients typically present with frequent sinopulmonary infections, but autoimmune, granulomatous, and lymphoproliferative diseases occur in a significant proportion [7]. Perhaps due to the heterogeneous nature and somewhat later onset of symptoms than many other primary immunodeficiencies, the diagnosis of CVID is often delayed many years due to poor recognition of the immune defect [8••].
The underlying pathogenesis leading to the immunological findings of CVID is poorly understood. Rare monogenic causes for the disorder have been identified, some instances involving genes easily linked to the B cell dysfunction that defines CVID while in other cases the connection to antibody deficiency is less clear [9]. Complicating genetics is that newly described autosomal dominant forms, such as mutations of cytotoxic T lymphocyte-associated protein 4 (CTLA-4), signal transducer and transcription activator 3 (STAT3), and NFκB1 are found in CVID subjects, but sometimes also in asymptomatic family members [10,11,12]. In other instances, genes such as transmembrane activator and calcium-modulating ligand interactor (TACI) found also in some normal subjects may act as disease modifiers rather than causative mutations [13]. Moreover, CVID is typically diagnosed in adulthood, suggesting a role for the environment, somatic genetic changes, and/or nucleic acid modification. Further research efforts are necessary to adequately understand the biology that underlies CVID and its complications.
CVID mortality has improved in recent decades due to wide adoption of IgG replacement therapy leading to reduction of infections, particularly severe examples such as meningitis, pneumonia, and sepsis [14,15,16,17]. Possibly due to this extended longevity, about half of CVID patients now suffer from complications unresponsive to IgG replacement [18]. These “non-infectious” complications are now the most important cause of morbidity and mortality in CVID and include autoimmune, gastrointestinal, and lung disease as well as malignancy [19•]. Treatment of these disorders in CVID is limited because their immunological basis is poorly understood. Simply put, it is not known why all CVID patients share the phenotype of profound antibody deficiency but not all develop these complications. Seeking to understand the reason for this major divergence in the clinical course of CVID, investigators have examined immunologic profiles, clinical phenotypes, cell populations and functions, molecular aspects, and cytokines (as reviewed [20••, 21, 22•]). The wide variability in clinical presentation, combined with the relative rarity of the disease and potential multiplicity of causes, are major hurdles to improve our understanding and develop better therapeutic strategies.
CVID Patients with Non-infectious Complications Have Distinctive Immunological Findings
Extensive work has been done to identify biological features distinguishing CVID patients with non-infectious complications from those without. Impairment of B cell maturation is a feature of many CVID patients, but it is most dramatically affected in CVID patients with these conditions. CVID patients with autoimmunity, granulomatous disease, lymphoid hyperplasia, or splenomegaly have significantly reduced numbers of isotype-switched memory B cells as compared to those without these complications [20••, 23, 24]. Another aspect of B cell dysfunction which specifically characterizes CVID patients with inflammatory complications is increased numbers of circulating CD21 low B cells, found especially in patients with autoimmunity and splenomegaly [25]. This B cell subset has self-reactivity but is apparently anergic and may have expanded in response to persistent antigenic stimulation, as increased numbers of these cells are also found in immunocompetent patients with autoimmune disease or chronic viral infection [26,27,28]. Autoimmunity, lymphoid hyperplasia, and splenomegaly are also more common in CVID patients with loss-of-function mutations in TACI, a receptor with an important role in B cell regulation [29, 30]. The B cells of these subjects, as well as mutation-bearing relatives, have similar dysfunctions in vitro [31]. Greater preservation of IgM production is associated with lymphoproliferative disease both benign and malignant and may be necessary for the development of at least some autoimmune manifestations in CVID [8••, 32]. In contrast, lower levels of serum IgM are linked with the development of bronchiectasis, a complication of chronic pulmonary bacterial infection [33,34,35,36,37,38]. While B cell impairment is a key feature of CVID, the mechanisms by which dysfunction of these lymphocytes occurs, and how such dysfunction is connected to the development of non-infectious complications remains to be elucidated.
Additional cellular defects have been identified in CVID over the years; not surprisingly, some of these have particularly associated with autoimmune or inflammatory complications. For example, autoimmunity appears more likely to occur in association with reduction of naïve and regulatory T cells in CVID [39,40,41,42,43]. Numerous defects in cytokine production as well as dendritic and other innate immune cell functions have also been characterized in CVID, potentially leading to the development of inflammatory features in some subjects [22•, 44,45,46]. Thus, the immune dysregulation underlying non-infectious complications in CVID clearly extends beyond B cell biology.
Interferon Signature in CVID Patients with Non-infectious Complications
A key observation in CVID is the fact that multiple autoimmune and inflammatory complications often occur in the same patient. For example, individual patients commonly have a history of autoimmune cytopenias, lymphoid hyperplasia, splenomegaly, and often granulomatous disease as well [20••, 32, 33]. In the largest retrospective analysis of 2212 CVID subjects, enteropathy was also associated with autoimmunity, granulomas, and splenomegaly, confirming a group of interrelated conditions [47]. This concurrence of complications in CVID hints at shared pathogenesis, or at least divergent effects of the same immunological dysfunction. For example, impaired B cell maturation or regulation, in the setting of lymphoid hyperplasia and loss of tolerance may give rise to autoimmune cytopenias [48,49,50,51,52]. In such patients, the B cell maturation defect could especially impair mucosal antibody defenses at this microbial interface and thereby predispose to enteropathy [53]. Yet, as mentioned earlier, B cell dysfunction may not be the only contributing factor for the emergence of non-infectious complications in CVID. Patients with mutations resulting in CTLA-4 haploinsufficiency, impairment of function of Fas and its receptor, or STAT-3 gain-of-function have all been linked to the development of autoimmunity, lymphoid hyperplasia, and splenomegaly in antibody deficient patients [10, 11, 54, 55]. Furthermore, association of granulomas with autoimmunity and lymphoid hyperplasia may be explained by the fact that granulomatous inflammation is a common pathology in settings of inadequate antigen clearance and excessive lymphoproliferation. Illustrating this fact, granulomatous inflammation is seen in biopsies of benign lymphoproliferation in patients regardless of a diagnosis of CVID [11, 56,57,58,59,60]. Thus, despite the diversity of conditions that emerge in CVID, unifying forms of immunological dysfunction underlying multiple non-infectious complications are likely.
Categorizing CVID patients into a simplified stratification on the basis of having non-infectious complications or not, our group previously compared the RNA expression profile of whole blood between these two categories of subjects. Interestingly, this study revealed that expression of interferon signature genes was significantly higher in CVID patients with these complications as compared to those without [61••]. While this study demonstrated an increase in the signature of genes common to type I and type II interferon pathways, our follow-up work clearly demonstrated a key role for interferon (IFN)-γ in inflammatory disease [62••]. INF-γ was first recognized for its importance in intracellular pathogen responses and has important stimulatory and modulatory effects upon other immune cells [63]. INF-γ is predominantly produced by conventional natural killer (NK) cells, natural killer T (NKT) cells, as well as effector CD4+ (Th1), and CD8+ (CTL) T cells. Unexpectedly, we found a significant expansion of circulating IFN-γ-producing innate lymphoid cells (ILCs) in CVID patients with non-infectious complications compared to those without and identified these cells in the affected mucosal tissues of these subjects [62••]. Identification of the expansion of ILCs in these CVID patients provided a novel area to further explore in the effort to understand the pathogenesis and clinical course of this primary immune deficiency.
Introduction to Innate Lymphoid Cell Biology
ILCs have recently emerged as innate-like counterparts of T lymphocytes, with similar activity and physiological roles as corresponding T cells [64•]. ILCs lack antigen specificity, produce a milieu of cytokines, and are enriched in barrier sites, such as skin and mucosal tissues. Thus, ILCs are endowed to respond locally and rapidly to environmental changes and act as a first-line modulator of immunity, inflammation, and tissue homeostasis. The ILC family has been divided in three different subclasses, based on shared developmental requirements and effector functions, in many cases mirroring that of effector T cell subsets (Table 1) [65••]. Thus, ILC-1 includes conventional natural killer (cNK) cells, CD127+ ILC-1s, and CD103+ intraephithelial ILC-1 (ieILC-1). cNKs and ieILC-1 have cytotoxic activity, mediated by perforin and granzyme B, while CD127+ ILC-1 have common progenitors and produce IFN-γ [66, 67]. Like Th1 cells, ILC-1 subsets have been implicated in immunity against intracellular bacteria and parasites [68]. ILC-2s are dependent on the transcription factor GATA3 and produce interleukin (IL)-5, IL-13, IL-9, and amphiregulin in response to IL-25 and IL-33 [69]. ILC-2 subsets have been linked to a rapid immune response to helminths and extracellular parasites as well as the development of allergic disease. ILC-3s are the most heterogeneous ILC group, yet they all share the necessity for the retinoic acid-related orphan receptor (ROR)γt, while further subdivided by their surface markers and transcription factor dependency [70]. Human ILC-3s have been shown to produce mainly tumor necrosis factor (TNF)-α, IL-22, IL-17, and in some cases IFN-γ.
Despite the established delineation of ILC subsets, these cells are in fact characterized by a great deal of plasticity, especially between ILC-1 and ILC-3s subsets. It has been shown that in humans, conversion of ILC-3s toward an ILC-1 phenotype is possible upon IL-15, IL-2, and IL-12 stimulation with concomitant inhibition of aryl hydrocarbon receptor signaling [71, 72]. The first study to report such plasticity demonstrated acquisition of T-bet with concomitant loss of RORγt expression in ILCs involved patients with Crohn’s disease who harbor an IL-17 and INF-γ producing cell population [73]. In addition, INF-γ producing ILC-1s could be generated in vitro from NKp44+ ILC-3s and ILC-1 cells expand within inflamed Crohn’s disease intestinal biopsies in correspondence with a loss of ILC-3 [74••, 75]. The natural cytotoxicity receptor NKp44 belongs to an Ig-like transmembrane activating receptor family on human NK cells, which has been also found in ILC subsets [71]. Expression of T-bet and IFN-γ in ILCs that expressed RORγt appears to be driven by IL-12 and IL-18, as well as, curiously, IL-1β and IL-23 [72, 74••]. This plasticity mirrors that of CD4+ T cells as Th2 and Th17 cells have been shown to acquire IFN-γ productive capacity in response to IL-12 and IL-23 stimulation [76]. The exact sequence of events by which ILC-3 lose RORγt and acquire features typical of ILC-1, such as T-bet expression, is still not fully understood [70].
ILCs and Inflammatory Diseases
As potent cytokine producers ILCs are now appreciated as key drivers of autoimmune and other forms of chronic inflammatory disease. Indeed, ILC activity is thought to underlie a variety of chronic inflammatory diseases, including inflammatory bowel disease, psoriasis, and rheumatic disease [77,78,79]. ILCs were first appreciated for their importance in immune regulation at mucosal sites. As such, distinct subsets of ILCs have been described in multiple tissues, particularly the gastrointestinal tract, lungs, and skin (for exhaustive review see [80]). Additionally, a significant role of ILCs is now also appreciated in lymphoid tissues such as tonsil and spleen (reviewed in [66, 81]).
Circulating ILCs may also play a distinct role in immune regulation [82]. It has been estimated that in healthy humans, about 0.01 to 0.1% of circulating lymphocytes express CD127, and most of these cells are ILC-2s [81]. More recently, another study has described a CD117+ circulating precursor for ILC cells in healthy humans [83]. However, it is becoming apparent that in various disease states different ILC subsets are enriched in circulation. Ren and colleagues first described a population of CD3− CD56+ NKp44+ CCR6+ cells reminiscent of ILC-3 with heightened frequency in both synovial fluid and peripheral blood of patients with rheumatoid arthritis [84]. Moreover, these ILC-3-like cells were found to produce IL-22 and TNF-α, which was correlated with disease activity [84]. IL-22 producing ILC-3s have also been described in circulation of patients with psoriasis, compared with numbers found in healthy individuals [85, 86]. Moreover, treatment with TNF-specific antibody in one psoriatic patient abrogated disease in association with a disappearance of NKp44+ ILC-3 cells from blood [86]. Similarly, lineage negative ILC-3-like cells have been found to be elevated in untreated multiple sclerosis patients. Interestingly, therapy with the IL-2 receptor antagonist daclizumab not only decreased the numbers of circulating ILCs in this disease but also modified their phenotype toward an immunoregulatory CD56bright NK lineage [87], providing an interesting insight on the plasticity of these cell types as well as their therapeutic potential. A similar population of regulatory CD56bright NKs has been also described in patients with systemic lupus erythematosus, although they did not correlate with disease activity [88]. Another ILC-3-like population has been described in patients with ankylosing spondylitis, a family of arthritis-associated inflammatory diseases. Phenotypically, they were defined as Lyn- RORc- T-bet+ and NKp44+ and capable of producing IL-17 and IL-22. These gut-derived ILC-3 were expanded in circulation, suggesting an active homing axis between the gut and the inflamed joints [89, 90]. Another type of complex and poorly understood autoimmune disease is systemic sclerosis, with patients showing altered frequencies of ILC-3 and ILC-1 in circulation [91], however, the clinical significance of these findings remain unclear.
ILC biology has just begun to be explored in CVID. A small study of 10 patients with CVID found decreased levels of mRNA levels for Th17-related genes, such as IL17, RORC2, and IL23R, which can also be expressed by ILCs [92]. In addition, lineage negative CD127+ CD90+ ILCs were decreased in peripheral blood of patients with CVID; however, no correlation with clinical features was described [92]. A more recent study found a decrease in CD117+ ILCs, mostly ILC-2, in the circulation of patients with CVID [93]. In the latter, patients with a more pronounced reduction of CD117+ ILCs also showed lower numbers of circulating marginal zone-like B cells and increased prevalence of chronic, non-infectious enteropathy [93]. We found an increase in IFN-γ-producing ILCs to be apparent when comparing CVID patients on the basis of whether or not they had non-infectious complications; those with such complications had increased levels of circulating ILC-3 cells [62••]. The diversity of these results speaks to the well-established heterogeneity of CVID that continues to complicate study of this primary immune deficiency. Further efforts will be needed to elucidate the mechanisms and significance of observations that ILC biology is altered in CVID to better understand how these immune cells influence the progression of this primary immune deficiency.
Our data suggests that ILCs play a prominent role as a source of IFN-γ that may promote the inflammation found in some subjects with CVID [61••]. Another group found that splenomegaly, one of the most common complications of CVID, was associated with an INFG polymorphism [94]. Along these lines, we found IFN-γ-expression to be a defining feature of the ILC-3 cells increased in these CVID patients, as cells were CD127+ and expressed intracellular IFN-γ as well as T-bet, the key transcription factor for IFN-γ-production [62••]. These results were similar to the IFN-γ-expressing pro-inflammatory ILC-3 population previously described in mice [67]. Indeed, murine studies have revealed that RORγt + T-bet + NKp46+ ILC-3s lose IL-17 producing capacity in favor of producing IFN-γ and IL-22 [67]. Thus, it is important to appreciate that a subset of ILC-3 cells may be an important source of IFN-γ during disease states, including in CVID.
Future Directions and Therapeutic Perspectives
As earlier mentioned, an upregulated interferon signature characterizes numerous chronic inflammatory diseases as it also does CVID patients with non-infectious complications. Unsurprisingly, the therapeutic potential of modulating this interferon signature has been explored in autoimmune diseases such as Sjogren’s syndrome and systemic lupus erythematosus (SLE). Much of this focus has been on type I interferons, but IFN-γ antagonism is considered to have therapeutic potential as well [95, 96]. For example, neutralization of IFN-γ was shown to ameliorate disease in a mouse model of SLE and IFN-γ antagonism was shown to downregulate IFN signature genes in SLE patients [97, 98]. However, downregulation of IFN signature genes mediated by therapeutic IFN-γ antagonism failed to coincide with clinical improvement in patients with discoid lupus [99]. Much work remains to be done in optimizing this therapeutic approach. Treatment that targets both type 1 IFN and IFN-γ signaling, through STAT inhibition or other methods, may be more effective than targeting one cytokine type alone given the redundancy of their effects [100].
ILC-3 cells themselves are also intriguing therapeutic targets in CVID. Some therapy already in use may have underappreciated roles in modulating ILC activity. For example, inflammatory cytokine production by ILC-3 cells is reduced by the immunosuppressant medication cyclosporin A [101]. Therapeutic antagonism of IL-23 may have benefits both by ameliorating the pathogenic effects of this cytokine as well as its role as a stimulus of IFN-γ production and ILC-3 activation [102]. In a short 8-week clinical trial, IL-23 blockade with risankizumab demonstrated efficacy for inducing remission of Crohn’s disease [103]. Therapeutic antagonisms of other cytokines, such as IL-1 or IL-6, may also suppress activation and expansion of ILC-3 cells. Alternatively, treatments impairing cell trafficking may have a profound effect on ILC-driven pathology, as these cells mediate much of their effects locally. Along these lines, as ILCs utilize the integrin α4β7 to migrate to the gastrointestinal tract, their depletion from the GI tract may, along with inhibition of T cell recruitment, contribute to the efficacy of vedolizumab in inflammatory bowel disease [104, 105]. Yet, the relative contribution of ILC-3 suppression to overall efficacy seen by these therapeutic approaches remains to be determined.
Numerous unique considerations regarding CVID remain to be understood in the pursuit of improved therapy for these patients. Prospective longitudinal studies of CVID are lacking in order to determine whether IFN signature expression or circulating ILC expansion precedes the development of inflammatory complications. While hematopoietic stem cell transplant (HSCT) has been used infrequently and with high mortality rates in CVID, efficacy has been profound in those that survive the treatment [106]. Thus, future advancements in HSCT patient selection and safety may improve outcomes in CVID and lead to greater usage of such treatment and consequently have effects upon cytokine and ILC dysregulation in these patients. Similarly, advancement of genetic diagnosis and corresponding gene therapy approaches may lead to future usage of this treatment in some cases of CVID. One of the hallmarks of ILCs is their enrichment in mucosal sites, as well as local self-renewal [107]. Thus, ILC reconstitution after HSCT is slow, as chemo and radiotherapy deplete blood ILCs. A study has shown that a circulating ILC-3 population reappeared after both chemotherapy and allogenic HSCT, but whether the contribution to pathogenesis of certain disease states would be ameliorated by such therapy is unknown [82]. The impact of HSCT and gene therapy upon ILC biology and pathogenic activities of these cells may ultimately have significant impact upon the therapeutic course of CVID, but important mechanisms of their pathogenesis remain to be elucidated.
Conclusions
The development of non-infectious complications in patients with CVID remains an enigma. While immunological findings associated with these complications are numerous, the pathogenesis is not clear. Recent identification of an increased IFN signature distinguishing CVID patients with non-infectious complications provides a promising avenue of further research because this finding is also shared with other chronic inflammatory diseases where it is being explored as a therapeutic target. Increased circulating ILCs were identified in CVID patients with non-infectious complications and may be an important driving force of the IFN signature also found to distinguish these patients. Of particular importance may be ILC-3 as a key source of pathogenic IFN-γ in CVID. Further research is needed to better understand the contribution of the IFN signature and expansion of IFN-γ-producing ILCs to non-infectious complications in CVID and assess their potential as therapeutic targets.
Numerous unanswered questions remain as ripe areas for future research. What is driving this IFN signature and ILC expansion in a subset of CVID patients? Extensive genetic studies of CVID have yet to reveal an explanation of upregulation of interferon genes. Alterations of the microbiota and translocation of bacterial products due to mucosal antibody deficiency of these patients may play a role, but this remains to be shown conclusively [108]. Moreover, how does the observed IFN signature gene dysregulation relate to the profound B cell dysfunction characterizing CVID? IFN has been shown to delete B cells in the setting of viral infection but has also been linked to the development of autoantibodies, so clearer delineation of the impact of IFN, and perhaps IFN-γ specifically, upon B cells remains to be defined [109, 110]. While early reports have hinted at the importance of IFN and ILC expansion for emergence of non-infectious complications in CVID, the area remains in need of greater research efforts in order to progress toward impactful clinical intervention.
References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
Cunningham-Rundles C, Maglione PJ. Common variable immunodeficiency. J Allergy Clin Immunol. 2012;129(5):1425–6. e3
Tseng CW, Lai KL, Chen DY, Lin CH, Chen HH. The incidence and prevalence of common variable immunodeficiency disease in Taiwan, A Population-Based Study. PLoS One. 2015;10(10):e0140473.
Chapel H, Cunningham-Rundles C. Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions. Br J Haematol. 2009;145(6):709–27.
Maffucci P, Filion CA, Boisson B, Itan Y, Shang L, Casanova JL, et al. Genetic diagnosis using whole exome sequencing in common variable immunodeficiency. Front Immunol. 2016;7:220.
Salzer U, Unger S, Warnatz K. Common variable immunodeficiency (CVID): exploring the multiple dimensions of a heterogeneous disease. Ann N Y Acad Sci. 2012;1250:41–9.
Bonilla FA, Barlan I, Chapel H, Costa-Carvalho BT, Cunningham-Rundles C, de la Morena MT, et al. International consensus document (ICON): common variable immunodeficiency disorders. J Allergy Clin Immunol Pract. 2016;4(1):38–59.
Maglione PJ. Autoimmune and lymphoproliferative complications of common variable immunodeficiency. Curr Allergy Asthma Rep. 2016;16(3):19.
•• Chapel H, Lucas M, Lee M, Bjorkander J, Webster D, Grimbacher B, et al. Common variable immunodeficiency disorders: division into distinct clinical phenotypes. Blood. 2008;112(2):277–86. The first report demonstrating increased mortality of CVID patients with non-infectious complications
Keller MD, Jyonouchi S. Chipping away at a mountain: genomic studies in common variable immunodeficiency. Autoimmun Rev. 2013;12(6):687–9.
Schubert D, Bode C, Kenefeck R, Hou TZ, Wing JB, Kennedy A, et al. Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations. Nat Med. 2014;20(12):1410–6.
Milner JD, Vogel TP, Forbes L, Ma CA, Stray-Pedersen A, Niemela JE, et al. Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations. Blood. 2015;125(4):591–9.
Kaustio M, Haapaniemi E, Goos H, Hautala T, Park G, Syrjanen J, et al. Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes. J Allergy Clin Immunol. 2017.
Lee JJ, Ozcan E, Rauter I, Geha RS. Transmembrane activator and calcium-modulator and cyclophilin ligand interactor mutations in common variable immunodeficiency. Curr Opin Allergy Clin Immunol. 2008;8(6):520–6.
Healy MJ. Hypogammaglobulinaemia in the United Kingdom. XII. Statistical analyses: prevalence, mortality and effects of treatment. Spec Rep Ser Med Res Counc (G B). 1971;310:115–23.
Cunningham-Rundles C, Bodian C. Common variable immunodeficiency: clinical and immunological features of 248 patients. Clin Immunol. 1999;92(1):34–48.
Busse PJ, Razvi S, Cunningham-Rundles C. Efficacy of intravenous immunoglobulin in the prevention of pneumonia in patients with common variable immunodeficiency. J Allergy Clin Immunol. 2002;109(6):1001–4.
Orange JS, Grossman WJ, Navickis RJ, Wilkes MM. Impact of trough IgG on pneumonia incidence in primary immunodeficiency: a meta-analysis of clinical studies. Clin Immunol. 2010;137(1):21–30.
Cunningham-Rundles C. The many faces of common variable immunodeficiency. Hematology Am Soc Hematol Educ Program. 2012;2012:301–5.
• Resnick ES, Moshier EL, Godbold JH, Cunningham-Rundles C. Morbidity and mortality in common variable immune deficiency over 4 decades. Blood. 2012;119(7):1650–7. Large single center US study demonstrating worsened survival of CVID patients with non-infectious complications
•• Wehr C, Kivioja T, Schmitt C, Ferry B, Witte T, Eren E, et al. The EUROclass trial: defining subgroups in common variable immunodeficiency. Blood. 2008;111(1):77–85. This report demonstrated specific immunological associations with the development of non-infectious complications as well as the fact that different non-infections complications are interrelated in CVID
Ochtrop ML, Goldacker S, May AM, Rizzi M, Draeger R, Hauschke D, et al. T and B lymphocyte abnormalities in bone marrow biopsies of common variable immunodeficiency. Blood. 2011;118(2):309–18.
• Varzaneh FN, Keller B, Unger S, Aghamohammadi A, Warnatz K, Rezaei N. Cytokines in common variable immunodeficiency as signs of immune dysregulation and potential therapeutic targets - a review of the current knowledge. J Clin Immunol. 2014;34(5):524–43. Review on cytokine dysregulation in CVID and the potential of therapy through immunomodulation
Abolhassani H, Amirkashani D, Parvaneh N, Mohammadinejad P, Gharib B, Shahinpour S, et al. Autoimmune phenotype in patients with common variable immunodeficiency. J Investig Allergol Clin Immunol. 2013;23(5):323–9.
Sanchez-Ramon S, Radigan L, Yu JE, Bard S, Cunningham-Rundles C. Memory B cells in common variable immunodeficiency: clinical associations and sex differences. Clin Immunol. 2008;128(3):314–21.
Warnatz K, Wehr C, Drager R, Schmidt S, Eibel H, Schlesier M, et al. Expansion of CD19(hi)CD21(lo/neg) B cells in common variable immunodeficiency (CVID) patients with autoimmune cytopenia. Immunobiology. 2002;206(5):502–13.
Isnardi I, Ng YS, Menard L, Meyers G, Saadoun D, Srdanovic I, et al. Complement receptor 2/CD21- human naive B cells contain mostly autoreactive unresponsive clones. Blood. 2010;115(24):5026–36.
Moir S, Ho J, Malaspina A, Wang W, DiPoto AC, O'Shea MA, et al. Evidence for HIV-associated B cell exhaustion in a dysfunctional memory B cell compartment in HIV-infected viremic individuals. J Exp Med. 2008;205(8):1797–805.
Terrier B, Joly F, Vazquez T, Benech P, Rosenzwajg M, Carpentier W, et al. Expansion of functionally anergic CD21−/low marginal zone-like B cell clones in hepatitis C virus infection-related autoimmunity. J Immunol. 2011;187(12):6550–63.
Zhang L, Radigan L, Salzer U, Behrens TW, Grimbacher B, Diaz G, et al. Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes. J Allergy Clin Immunol. 2007;120(5):1178–85.
Salzer U, Chapel HM, Webster AD, Pan-Hammarstrom Q, Schmitt-Graeff A, Schlesier M, et al. Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans. Nat Genet. 2005;37(8):820–8.
Martinez-Gallo M, Radigan L, Almejun MB, Martinez-Pomar N, Matamoros N, Cunningham-Rundles C. TACI mutations and impaired B-cell function in subjects with CVID and healthy heterozygotes. J Allergy Clin Immunol. 2013;131(2):468–76.
Maglione PJ, Overbey JR, Radigan L, Bagiella E, Cunningham-Rundles C. Pulmonary radiologic findings in common variable immunodeficiency: clinical and immunological correlations. Ann Allergy Asthma Immunol. 2014;113(4):452–9.
Gathmann B, Mahlaoui N, Ceredih, Gerard L, Oksenhendler E, Warnatz K, et al. Clinical picture and treatment of 2212 patients with common variable immunodeficiency. J Allergy Clin Immunol. 2014;134(1):116–26.
Gobert D, Bussel JB, Cunningham-Rundles C, Galicier L, Dechartres A, Berezne A, et al. Efficacy and safety of rituximab in common variable immunodeficiency-associated immune cytopenias: a retrospective multicentre study on 33 patients. Br J Haematol. 2011;155(4):498–508.
Boursiquot JN, Gerard L, Malphettes M, Fieschi C, Galicier L, Boutboul D, et al. Granulomatous disease in CVID: retrospective analysis of clinical characteristics and treatment efficacy in a cohort of 59 patients. J Clin Immunol. 2013;33(1):84–95.
Hill F, Yonkof J, Chaitanya Arudra SK, Thomas J, Altorok N. Successful Treatment of ANCA-associated vasculitis in the setting of common variable immunodeficiency using rituximab. Am J Ther. 2016;23(5):e1239–45.
Maglione PJ, Ko HM, Beasley MB, Strauchen JA, Cunningham-Rundles C. Tertiary lymphoid neogenesis is a component of pulmonary lymphoid hyperplasia in patients with common variable immunodeficiency. J Allergy Clin Immunol. 2014;133(2):535–42.
Chase NM, Verbsky JW, Hintermeyer MK, Waukau JK, Tomita-Mitchell A, Casper JT, et al. Use of combination chemotherapy for treatment of granulomatous and lymphocytic interstitial lung disease (GLILD) in patients with common variable immunodeficiency (CVID). J Clin Immunol. 2013;33(1):30–9.
Oraei M, Aghamohammadi A, Rezaei N, Bidad K, Gheflati Z, Amirkhani A, et al. Naive CD4+ T cells and recent thymic emigrants in common variable immunodeficiency. J Investig Allergol Clin Immunol. 2012;22(3):160–7.
Carter CR, Aravind G, Smalle NL, Cole JY, Savic S, Wood PM. CVID patients with autoimmunity have elevated T cell expression of granzyme B and HLA-DR and reduced levels of Treg cells. J Clin Pathol. 2013;66(2):146–50.
Arandi N, Mirshafiey A, Jeddi-Tehrani M, Abolhassani H, Sadeghi B, Mirminachi B, et al. Evaluation of CD4+CD25+FOXP3+ regulatory T cells function in patients with common variable immunodeficiency. Cell Immunol. 2013;281(2):129–33.
Arandi N, Mirshafiey A, Abolhassani H, Jeddi-Tehrani M, Edalat R, Sadeghi B, et al. Frequency and expression of inhibitory markers of CD4(+) CD25(+) FOXP3(+) regulatory T cells in patients with common variable immunodeficiency. Scand J Immunol. 2013;77(5):405–12.
Genre J, Errante PR, Kokron CM, Toledo-Barros M, Camara NO, Rizzo LV. Reduced frequency of CD4(+)CD25(HIGH)FOXP3(+) cells and diminished FOXP3 expression in patients with common variable immunodeficiency: a link to autoimmunity? Clin Immunol. 2009;132(2):215–21.
Yu JE, Zhang L, Radigan L, Sanchez-Ramon S, Cunningham-Rundles C. TLR-mediated B cell defects and IFN-alpha in common variable immunodeficiency. J Clin Immunol. 2012;32(1):50–60.
Sharifi L, Tavakolinia N, Kiaee F, Rezaie N, Mohsenzadegan M, Shariat M, et al. A review on defects of dendritic cells in common variable immunodeficiency. Endocr Metab Immune Disord Drug Targets. 2017;17(2):100–113.
Knight AK, Radigan L, Marron T, Langs A, Zhang L, Cunningham-Rundles C. High serum levels of BAFF, APRIL, and TACI in common variable immunodeficiency. Clin Immunol. 2007;124(2):182–9.
Gathmann B, Mahlaoui N, Gerard L, Oksenhendler E, Warnatz K, Schulze I, et al. Clinical picture and treatment of 2212 patients with common variable immunodeficiency. J Allergy Clin Immunol. 2014;134(1):116–26.
Seidel MG. Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatment. Blood. 2014;124(15):2337–44.
Roskin KM, Simchoni N, Liu Y, Lee JY, Seo K, Hoh RA, et al. IgH sequences in common variable immune deficiency reveal altered B cell development and selection. Sci Transl Med. 2015;7(302):302ra135.
Daridon C, Loddenkemper C, Spieckermann S, Kuhl AA, Salama A, Burmester GR, et al. Splenic proliferative lymphoid nodules distinct from germinal centers are sites of autoantigen stimulation in immune thrombocytopenia. Blood. 2012;120(25):5021–31.
Franchini M, Vescovi PP, Garofano M, Veneri D. Helicobacter pylori-associated idiopathic thrombocytopenic purpura: a narrative review. Semin Thromb Hemost. 2012;38(5):463–8.
Romberg N, Chamberlain N, Saadoun D, Gentile M, Kinnunen T, Ng YS, et al. CVID-associated TACI mutations affect autoreactive B cell selection and activation. J Clin Invest. 2013;123(10):4283–93.
Jorgensen SF, Reims HM, Frydenlund D, Holm K, Paulsen V, Michelsen AE, et al. A cross-sectional study of the prevalence of gastrointestinal symptoms and pathology in patients with common variable immunodeficiency. Am J Gastroenterol. 2016;111(10):1467–75.
Rensing-Ehl A, Warnatz K, Fuchs S, Schlesier M, Salzer U, Draeger R, et al. Clinical and immunological overlap between autoimmune lymphoproliferative syndrome and common variable immunodeficiency. Clin Immunol. 2010;137(3):357–65.
Kuehn HS, Ouyang W, Lo B, Deenick EK, Niemela JE, Avery DT, et al. Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4. Science. 2014;345(6204):1623–7.
de Jager M, Blokx W, Warris A, Bergers M, Link M, Weemaes C, et al. Immunohistochemical features of cutaneous granulomas in primary immunodeficiency disorders: a comparison with cutaneous sarcoidosis. J Cutan Pathol. 2008;35(5):467–72.
Unger S, Seidl M, Schmitt-Graeff A, Bohm J, Schrenk K, Wehr C, et al. Ill-defined germinal centers and severely reduced plasma cells are histological hallmarks of lymphadenopathy in patients with common variable immunodeficiency. J Clin Immunol. 2014;34(6):615–26.
Reddy DL, Venter WD, Pather S. Patterns of lymph node pathology; fine needle aspiration biopsy as an evaluation tool for lymphadenopathy: a retrospective descriptive study conducted at the largest Hospital in Africa. PLoS One. 2015;10(6):e0130148.
Ko HM, da Cunha SG, Darling G, Pierre A, Yasufuku K, Boerner SL, et al. Diagnosis and subclassification of lymphomas and non-neoplastic lesions involving mediastinal lymph nodes using endobronchial ultrasound-guided transbronchial needle aspiration. Diagn Cytopathol. 2013;41(12):1023–30.
Tian X, Yi ES, Ryu JH. Lymphocytic interstitial pneumonia and other benign lymphoid disorders. Semin Respir Crit Care Med. 2012;33(5):450–61.
•• Park J, Munagala I, Xu H, Blankenship D, Maffucci P, Chaussabel D, et al. Interferon signature in the blood in inflammatory common variable immune deficiency. PLoS One. 2013;8(9):e74893. Report of heightened expression of interferon signature genes distinguishing CVID patients with non-infectious complications.
•• Cols M, Rahman A, Maglione PJ, Garcia-Carmona Y, Simchoni N, Ko HB, et al. Expansion of inflammatory innate lymphoid cells in patients with common variable immune deficiency. J Allergy Clin Immunol. 2016;137(4):1206–15. e1-6. Identification of increased circulating innate lymphoid cells producing IFN-γ in CVID with inflammatory complications
Smith NL, Denning DW. Clinical implications of interferon-gamma genetic and epigenetic variants. Immunology. 2014;143(4):499–511.
• Klose CS, Artis D. Innate lymphoid cells as regulators of immunity, inflammation and tissue homeostasis. Nat Immunol. 2016;17(7):765–74. Detailed review of innate lymphoid cell biology
•• Lim AI, Verrier T, Vosshenrich CA, Di Santo JP. Developmental options and functional plasticity of innate lymphoid cells. Curr Opin Immunol. 2017;44:61–8. Review of the plasticity of innate lymphoid cells.
Juelke K, Romagnani C. Differentiation of human innate lymphoid cells (ILCs). Curr Opin Immunol. 2016;38:75–85.
Robinette ML, Colonna M. Immune modules shared by innate lymphoid cells and T cells. J Allergy Clin Immunol. 2016;138(5):1243–51.
Jiao Y, Huntington ND, Belz GT, Seillet C. Type 1 innate lymphoid cell biology: lessons learnt from natural killer cells. Front Immunol. 2016;7:426.
Roediger B, Weninger W. Group 2 innate lymphoid cells in the regulation of immune responses. Adv Immunol. 2015;125:111–54.
Montaldo E, Juelke K, Romagnani C. Group 3 innate lymphoid cells (ILC3s): origin, differentiation, and plasticity in humans and mice. Eur J Immunol. 2015;45(8):2171–82.
Cella M, Otero K, Colonna M. Expansion of human NK-22 cells with IL-7, IL-2, and IL-1beta reveals intrinsic functional plasticity. Proc Natl Acad Sci U S A. 2010;107(24):10961–6.
Vonarbourg C, Mortha A, Bui VL, Hernandez PP, Kiss EA, Hoyler T, et al. Regulated expression of nuclear receptor RORgammat confers distinct functional fates to NK cell receptor-expressing RORgammat(+) innate lymphocytes. Immunity. 2010;33(5):736–51.
Annunziato F, Cosmi L, Santarlasci V, Maggi L, Liotta F, Mazzinghi B, et al. Phenotypic and functional features of human Th17 cells. J Exp Med. 2007;204(8):1849–61.
•• Bernink JH, Peters CP, Munneke M, te Velde AA, Meijer SL, Weijer K, et al. Human type 1 innate lymphoid cells accumulate in inflamed mucosal tissues. Nat Immunol. 2013;14(3):221–9. Demonstration of the plasticity of ILC-1 and ILC-3 subsets.
Bernink JH, Krabbendam L, Germar K, de Jong E, Gronke K, Kofoed-Nielsen M, et al. Interleukin-12 and -23 control plasticity of CD127(+) group 1 and group 3 innate lymphoid cells in the intestinal lamina Propria. Immunity. 2015;43(1):146–60.
Gaffen SL, Jain R, Garg AV, Cua DJ. The IL-23-IL-17 immune axis: from mechanisms to therapeutic testing. Nat Rev Immunol. 2014;14(9):585–600.
Forkel M, Mjosberg J. Dysregulation of group 3 innate lymphoid cells in the pathogenesis of inflammatory bowel disease. Curr Allergy Asthma Rep. 2016;16(10):73.
Mjosberg J, Eidsmo L. Update on innate lymphoid cells in atopic and non-atopic inflammation in the airways and skin. Clin Exp Allergy. 2014;44(8):1033–43.
Yazdani R, Sharifi M, Shirvan AS, Azizi G, Ganjalikhani-Hakemi M. Characteristics of innate lymphoid cells (ILCs) and their role in immunological disorders (an update). Cell Immunol. 2015;298(1–2):66–76.
Artis D, Spits H. The biology of innate lymphoid cells. Nature. 2015;517(7534):293–301.
Hazenberg MD, Spits H. Human innate lymphoid cells. Blood. 2014;124(5):700–9.
Munneke JM, Bjorklund AT, Mjosberg JM, Garming-Legert K, Bernink JH, Blom B, et al. Activated innate lymphoid cells are associated with a reduced susceptibility to graft-versus-host disease. Blood. 2014;124(5):812–21.
Lim AI, Li Y, Lopez-Lastra S, Stadhouders R, Paul F, Casrouge A, et al. Systemic human ILC precursors provide a substrate for tissue ILC differentiation. Cell. 2017;168(6):1086–100. e10
Ren J, Feng Z, Lv Z, Chen X, Li J. Natural killer-22 cells in the synovial fluid of patients with rheumatoid arthritis are an innate source of interleukin 22 and tumor necrosis factor-alpha. J Rheumatol. 2011;38(10):2112–8.
Teunissen MB, Munneke JM, Bernink JH, Spuls PI, Res PC, Te Velde A, et al. Composition of innate lymphoid cell subsets in the human skin: enrichment of NCR(+) ILC3 in lesional skin and blood of psoriasis patients. J Invest Dermatol. 2014;134(9):2351–60.
Villanova F, Flutter B, Tosi I, Grys K, Sreeneebus H, Perera GK, et al. Characterization of innate lymphoid cells in human skin and blood demonstrates increase of NKp44+ ILC3 in psoriasis. J Invest Dermatol. 2014;134(4):984–91.
Perry JS, Han S, Xu Q, Herman ML, Kennedy LB, Csako G, et al. Inhibition of LTi cell development by CD25 blockade is associated with decreased intrathecal inflammation in multiple sclerosis. Sci Transl Med. 2012;4(145):145ra106.
Schepis D, Gunnarsson I, Eloranta ML, Lampa J, Jacobson SH, Karre K, et al. Increased proportion of CD56bright natural killer cells in active and inactive systemic lupus erythematosus. Immunology. 2009;126(1):140–6.
Ciccia F, Accardo-Palumbo A, Alessandro R, Rizzo A, Principe S, Peralta S, et al. Interleukin-22 and interleukin-22-producing NKp44+ natural killer cells in subclinical gut inflammation in ankylosing spondylitis. Arthritis Rheum. 2012;64(6):1869–78.
Ciccia F, Guggino G, Rizzo A, Saieva L, Peralta S, Giardina A, et al. Type 3 innate lymphoid cells producing IL-17 and IL-22 are expanded in the gut, in the peripheral blood, synovial fluid and bone marrow of patients with ankylosing spondylitis. Ann Rheum Dis. 2015;74(9):1739–47.
Roan F, Stoklasek TA, Whalen E, Molitor JA, Bluestone JA, Buckner JH, et al. CD4+ group 1 innate lymphoid cells (ILC) form a functionally distinct ILC subset that is increased in systemic sclerosis. J Immunol. 2016;196(5):2051–62.
Ganjalikhani-Hakemi M, Yazdani R, Sherkat R, Homayouni V, Masjedi M, Hosseini M. Evaluation of the T helper 17 cell specific genes and the innate lymphoid cells counts in the peripheral blood of patients with the common variable immunodeficiency. J Res Med Sci. 2014;19(Suppl 1):S30–5.
Geier CB, Kraupp S, Bra D, Eibl MM, Farmer JR, Csomos K, et al. Reduced numbers of circulating group 2 innate lymphoid cells in patients with common variable immunodeficiency. Eur J Immunol. 2017.
Perovic D, Perovic V, Pravica V, Bonaci-Nikolic B, Mijanovic R, Bunjevacki V. Evaluation of cytokine genetic polymorphisms in adult patients with common variable immunodeficiency: a single-center study. Immunol Lett. 2016;176:97–104.
Ronnblom L. The importance of the type I interferon system in autoimmunity. Clin Exp Rheumatol. 2016;34(4 Suppl 98):21–4.
Oon S, Wilson NJ, Wicks I. Targeted therapeutics in SLE: emerging strategies to modulate the interferon pathway. Clin Transl Immunol. 2016;5(5):e79.
Gottschalk TA, Tsantikos E, Hibbs ML. Pathogenic inflammation and its therapeutic targeting in systemic lupus Erythematosus. Front Immunol. 2015;6:550.
Welcher AA, Boedigheimer M, Kivitz AJ, Amoura Z, Buyon J, Rudinskaya A, et al. Blockade of interferon-gamma normalizes interferon-regulated gene expression and serum CXCL10 levels in patients with systemic lupus erythematosus. Arthritis Rheumatol. 2015;67(10):2713–22.
Werth VP, Fiorentino D, Sullivan BA, Boedigheimer MJ, Chiu K, Wang C, et al. Brief report: pharmacodynamics, safety, and clinical efficacy of AMG 811, a human anti-interferon-gamma antibody, in patients with discoid lupus Erythematosus. Arthritis Rheumatol. 2017;69(5):1028–34.
Goropevsek A, Holcar M, Avcin T. The role of STAT signaling pathways in the pathogenesis of systemic lupus Erythematosus. Clin Rev Allergy Immunol. 2017;52(2):164–81.
Glatzer T, Killig M, Meisig J, Ommert I, Luetke-Eversloh M, Babic M, et al. RORgammat(+) innate lymphoid cells acquire a proinflammatory program upon engagement of the activating receptor NKp44. Immunity. 2013;38(6):1223–35.
Goldberg R, Prescott N, Lord GM, Mac Donald TT, Powell N. The unusual suspects--innate lymphoid cells as novel therapeutic targets in IBD. Nat Rev Gastroenterol Hepatol. 2015;12(5):271–83.
Feagan BG, Sandborn WJ, D'Haens G, Panes J, Kaser A, Ferrante M, et al. Induction therapy with the selective interleukin-23 inhibitor risankizumab in patients with moderate-to-severe Crohn's disease: a randomised, double-blind, placebo-controlled phase 2 study. Lancet. 2017;389(10080):1699–709.
Rivera-Nieves J. Strategies that target leukocyte traffic in inflammatory bowel diseases: recent developments. Curr Opin Gastroenterol. 2015;31(6):441–8.
Ishizuka IE, Chea S, Gudjonson H, Constantinides MG, Dinner AR, Bendelac A, et al. Single-cell analysis defines the divergence between the innate lymphoid cell lineage and lymphoid tissue-inducer cell lineage. Nat Immunol. 2016;17(3):269–76.
Wehr C, Gennery AR, Lindemans C, Schulz A, Hoenig M, Marks R, et al. Multicenter experience in hematopoietic stem cell transplantation for serious complications of common variable immunodeficiency. J Allergy Clin Immunol. 2015;135(4):988–97.e6.
Fan X, Rudensky AY. Hallmarks of tissue-resident lymphocytes. Cell. 2016;164(6):1198–211.
Berbers RM, Nierkens S, van Laar JM, Bogaert D, Leavis HL. Microbial Dysbiosis in common variable immune deficiencies: evidence, causes, and consequences. Trends Immunol. 2017;38(3):206–16.
Fallet B, Narr K, Ertuna YI, Remy M, Sommerstein R, Cornille K, et al. Interferon-driven deletion of antiviral B cells at the onset of chronic infection. Sci Immunol. 2016;1(4).pii:eaah6817.
Castaneda-Delgado JE, Bastian-Hernandez Y, Macias-Segura N, Santiago-Algarra D, Castillo-Ortiz JD, Aleman-Navarro AL, et al. Type I interferon gene response is increased in early and established rheumatoid arthritis and correlates with autoantibody production. Front Immunol. 2017;8:285.
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Maglione, P.J., Cols, M. & Cunningham-Rundles, C. Dysregulation of Innate Lymphoid Cells in Common Variable Immunodeficiency. Curr Allergy Asthma Rep 17, 77 (2017). https://doi.org/10.1007/s11882-017-0746-6
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DOI: https://doi.org/10.1007/s11882-017-0746-6