Abstract
Immune thrombocytopenic purpura is an acquired autoimmune disorder that is the most common cause of thrombocytopenia in children. The endocannabinoid system is involved in immune regulation. We evaluated a common missense variant (CAA/CGG; Q63R) of the gene encoding the cannabinoid receptor type 2 (GeneID 1269) in 190 children with immune thrombocytopenic purpura and 600 healthy controls. The allelic frequencies and genotype distribution of the polymorphism in the patients were significant compared to control samples (P=0.006 and P=0.0001, respectively). Interestingly, when acute and chronic immune thrombocytopenic purpura patients were analyzed separately with respect to controls, a significant overrepresentation of the RR genotype and of the R allele was observed only for the chronic form (P=0.00021 and P=0.011, respectively). The relative odds ratio suggested the risk of developing chronic form was more than double in immune thrombocytopenic purpura children homozygous for the variant (odds ratio=2.349, 95% CI: 1.544–3.573; P<0.001).Introduction
Idiopathic thrombocytopenic purpura (ITP) is an autoimmune disorder characterized by thrombocytopenia (peripheral blood platelet count < 150×10/L) due to autoantibody binding to platelet antigen(s) causing their premature destruction by the reticuloendothelial system, particularly in the spleen.1 ITP diagnosis is based on low platelet number in the absence of other hematologic abnormalities or other causes of thrombocytopenia.2 The annual incidence of pediatric ITP is about 4 to 6 cases per 100,000. About 50% of childhood ITP cases show an acute onset following a viral or bacterial infection that commonly resolves within weeks to months without treatment. Nevertheless, about one fourth of these patients go on to develop a chronic disease, defined by a platelet count less than 150×10/L at six months after diagnosis.3,4
Although the immunopathogenesis of ITP is autoantibody-mediated, the exact mechanism of immune dysfunction is not known. However, there is substantial evidence to suggest that T cells and their cytokines play a pivotal role in the control of antiplatelet autoantibodies.5,6 A number of T-cell abnormalities have been demonstrated in patients with ITP and three main mechanisms have been hypothesized: i) a T-helper (Th)1 bias compared with Th2, particularly in chronic ITP; ii) the release of cytokines that interfere with megakaryocyte maturation and/or platelet release; and iii) a direct cytotoxic effect of T cells.7
T cells, as well as all other cellular components of the immune system, express cannabinoid receptors type 1 and 2 (CB1 and CB2). The endocannabinoid system is also involved in immune regulation by suppressing cell activation, modulating Th1 and Th2 balance, and inhibiting pro-inflammatory cytokine production.8–10 CB2 is encoded by the CNR2 gene, mapping on 1p36.11 (GeneID 1269; GenBank: #NM_001841.2), and is expressed at 10- to 100-fold greater levels than the CB1 on immune cells, including T lymphocytes, B cells, macrophages and neutrophils.10 Genome scan studies revealed a key role of the 1p36 region in different autoimmune diseases, such as rheumatoid arthritis,11 systemic lupus erythematosus,12 and type 1 diabetes.13
In this study, we show the CNR2 gene variation rs35761398 (Q63R) is significantly associated with childhood chronic ITP.
Design and Methods
Patients
The study included 190 (99 females) unrelated Italian children (median age 7 years; range 0.3–15.5) with ITP referred from March 1995 to December 2009 to the Department of Pediatrics of the Second University of Naples. Diagnosis and treatment of ITP were made according to the guidelines of the American Society of Hematology (ASH)14 and the Italian Association of Pediatric Hematology and Oncology (AIEOP).15,16 Thrombocytopenia that resolved within six months of onset was defined as acute ITP; while persistence of thrombocytopenia for longer than six months was defined as chronic ITP. Six hundred healthy Italian children (325 female, median age 9.7 years; range 1.8–13.8) served as controls. Controls, matched for age and sex, were recruited from the same geographical areas as ITP patients. These controls did not have a history of hematologic disorders of any kind. Clinical data are summarized in Table 1.
The study was approved by the Medical Ethics Committee of the Second University of Naples and was performed in accordance with the Declaration of Helsinki. Written informed consent was obtained from all patients’ parents prior to participation in the study.
Molecular study
Genomic DNA was extracted from peripheral whole blood. The CNR2 rs35761398 polymorphism was studied by polymerase chain reaction (PCR) followed by direct sequencing. The PCR conditions were: 94° C for 4 min followed by 31 cycles consisting of 94° C for 30 s, 60° C for 30 s, and 72° C for 30 s. Primers were chosen using Primer3 software (Forward: 5’-GAGTGGTCCCCAGAA-GACAG-3’; Reverse: 5’-CACAGAGGCTGTGAAGGTCA-3’). Amplimers were analyzed by direct sequencing using an ABI PRISM 310 automated sequencer (Applied Biosystem, Foster City, CA, USA) and the relative genotypes were assigned. The χ test was used to assess differences in genotype and allelic frequencies. The odds ratio for genotype distributions was calculated using SAS software. P values less than 0.05 were considered significant.
Results and Discussion
In total, 190 ITP children were evaluated, divided into acute (n=86, female 45%) and chronic (n=104, female 58%) ITP (Table 1). The number of patients recruited with chronic ITP was greater because the hospital where the study was carried out is the childhood ITP referral center for the Campania region of southern Italy. All patients were genotyped for the CNR2 rs35761398 variant, which changes the second and third adenosine at codon 63 (CAA) to guanosine (CGG) leading to the missense variant Q63R in the first intracellular signaling loop of the encoded CB2 protein. The allelic frequencies and the genotype distributions in controls and ITP patients are shown in Table 2. Whereas the allele frequencies in the controls were distributed according to Hardy-Weinberg (P=0.318) and were comparable to previously reported distributions,17 this was not the case in the ITP patients (P=7.069 × 10). Indeed, there were significant differences in allelic frequencies and genotype distribution in ITP patients compared to control samples (P=0.006 and P=0.0001, respectively) (Table 2). In addition, the relative odds ratio (OR) suggested a double risk of developing ITP in RR homozygous children with respect to QR heterozygous and QQ homozygous children (OR=2.006 95% CI 1.441–2.795; P<10) (Table 3).
Interestingly, when acute and chronic ITP patients were analyzed separately in comparison with controls, a significant overrepresentation of the RR genotype and of the R allele was observed only for the chronic form (P=0.00021 and P=0.011, respectively) (Table 2). Furthermore, the associated risk of developing chronic ITP increased more than two-fold for RR homozygous children (OR=2.349 95% CI 1.544–3.573; P<10) (Table 3). The genotype and allele distribution in acute ITP patients was comparable to the control samples (Table 2). Patient’s sex, the presence of autoimmune diseases, and platelet-associated antibodies were not significantly influenced by the CNR2 rs35761398 variant (Table 2).
This case-control association study aimed to explore the molecular determinants that influence the susceptibility to ITP in childhood. For the first time, we showed an association between ITP and a functional variant of the CNR2 gene, encoding for a protein known to affect immune function. The rationale for our study was based on: i) the linkage between the 1p36 locus, where CNR2 maps, and several autoimmune diseases; ii) the immunomodulating effect of CB2; and (iii) the evidence of abnormal autoreactive T-cell activation in chronic ITP. Cannabinoid ligands, acting on CB2 receptors expressed by immune cells, can inhibit cytokine production, decrease antigen presentation, modulate cell migration, and mediate suppressive effects on effectors.18,19 Furthermore, immunomodulation by cannabinoids is totally absent in mice lacking the CB2 receptor.20
The Q63R CB2 variant results in the amino acid substitution of a polar, uncharged, glutamine with a positively charged arginine. This change could affect the CB2 tertiary structure, altering the immunomodulating properties of CB2. It has been shown that human T cells from CB2 R63 homozygotes show a two-fold reduction in endocannabi-noid-induced inhibition of proliferation with respect to cells from CB2 Q63 homozygotes.21 Although the immunopathogenic cause of ITP has not yet been clarified, there is overwhelming evidence to suggest that a generalized dysfunction of autoreactive T cells could represent the critical immunopathological factor in chronic ITP.
Data presented in this study confirm the role of CB2 in autoimmunity susceptibility and reveal a significant and previously unknown association between CB2 and childhood ITP. However, other studies are needed before the CB2 receptor, localized on immune effector cells, is considered an eligible molecular target to modulate autoreactive, innate, and adaptive immune responses in the chronic form of ITP.
Acknowledgments
The authors would like to thank all patients and their families for their participation in the study.
Footnotes
- Funding: this work was supported by grants from “Progetti di Rilevante Interesse Nazionale” (PRIN, 2008), Regione Campania (L.R. 5/02, 2005), and the “Francesco Fede” Department of the Second University of Naples (Grant on Normal and Pathological Hematopoiesis).
- Authorship and Disclosures The information provided by the authors about contributions from persons listed as authors and in acknowledgments is available with the full text of this paper at www.haematologica.org.
- Financial and other disclosures provided by the authors using the ICMJE (www.icmje.org) Uniform Format for Disclosure of Competing Interests are also available at www.haematologica.org.
- Received April 11, 2011.
- Revision received July 21, 2011.
- Accepted August 2, 2011.
References
- Cooper N, Bussel J. The pathogenesis of immune thrombocytopaenic purpura. Br J Haematologica. 2006; 133(4):364-74. https://doi.org/10.1111/j.1365-2141.2006.06024.xGoogle Scholar
- Cines DB, Bussel JB, Liebman HA, Luning Prak ET. The ITP syndrome: pathogenic and clinical diversity. Blood. 2009; 113(26):6511-21. PubMedhttps://doi.org/10.1182/blood-2009-01-129155Google Scholar
- Bergmann AK, Grace RF, Neufeld EJ. Genetic studies in pediatric ITP: outlook, feasibility, and requirements. Ann Hematol. 2010; 89(Suppl 1):S95-103. PubMedGoogle Scholar
- Breunis WB, van Mirre E, Bruin M, Geissler J, de Boer M, Peters M. Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura. Blood. 2008; 111(3):1029-38. PubMedhttps://doi.org/10.1182/blood-2007-03-079913Google Scholar
- Kuwana M, Ikeda Y. The role of autoreactive T-cells in the pathogenesis of idiopathic thrombocytopenic purpura. Int J Hematol. 2005; 81(2):106-12. PubMedhttps://doi.org/10.1532/IJH97.04176Google Scholar
- Ouzaki A, Theodoropoulou M, Gianakopoulos I, Vlaha V, Kyrtsonis MC, Maniatis A. Expression patterns of Th1 and Th2 cytokine genes in childhood idiopathic thrombocytopenic purpura (ITP) at presentation and their modulation by intravenous immunoglobulin G (IVIg) treatment: their role in prognosis. Blood. 2002; 100(5):1774-9. PubMedGoogle Scholar
- Wang T, Zhao H, Ren H, Guo J, Xu M, Yang R. Type 1 and type 2 T-cell profiles in idiopathic thrombocytopenic purpura. Haematologica. 2005; 90(7):914-23. PubMedGoogle Scholar
- Galiègue S, Mary S, Marchand J, Dussossoy D, Carrière D, Carayon P. Expression of central and peripheral cannabinoid receptors in human immune tissues and leukocyte sub-populations. Eur J Biochem. 1995; 232(1):54-61. PubMedGoogle Scholar
- Cabral GA, Griffin-Thomas L. Emerging role of the cannabinoid receptor CB2 in immune regulation: therapeutic prospects for neuroinflammation. Expert Rev Mol Med. 2009; 11:e3. PubMedhttps://doi.org/10.1017/S1462399409000957Google Scholar
- Cencioni MT, Chiurchiù V, Catanzaro G, Borsellino G, Bernardi G, Battistini L. Anandamide suppresses proliferation and cytokine release from primary human T-lymphocytes mainly via CB2 receptors. PLoS One. 2010; 5(1):e8688. PubMedhttps://doi.org/10.1371/journal.pone.0008688Google Scholar
- Osawa K, Takami N, Shiozawa K, Hashiramoto A, Shiozawa S. Death receptor 3 (DR3) gene duplication in a chromosome region 1p36.3: gene duplication is more prevalent in rheumatoid arthritis. Genes Immun. 2004; 5(6):439-43. PubMedhttps://doi.org/10.1038/sj.gene.6364097Google Scholar
- Shai R, Quismorio FP, Li L, Kwon OJ, Morrison J, Wallace DJ. Genome-wide screen for systemic lupus erythematosus susceptibility genes in multiplex families. Hum Mol Genet. 1999; 8(4):639-44. PubMedhttps://doi.org/10.1093/hmg/8.4.639Google Scholar
- Nishimura M, Obayashi H, Mizuta I, Hara H, Adachi T, Ohta M. TNF, TNF Receptor Type 1, and Allograft Inflammatory Factor-1 Gene Polymorphisms in Japanese Patients With Type 1. Diab Hum Immunol. 2003; 64(2):302-9. https://doi.org/10.1016/S0198-8859(02)00799-1Google Scholar
- George JN, Woolf SH, Raskob GE. Idiopathic thrombocytopenic purpura: a guideline for diagnosis and management of children and adults. American Society of Hematology. Ann Med. 1998; 30(1):38-44. PubMedGoogle Scholar
- De Mattia D, Del Principe D, Del Vecchio GC, Jankovic M, Arrighini A, Giordano P. Acute childhood idiopathic thrombocytopenic purpura: AIEOP consensus guidelines for diagnosis and treatment. Associazione Italiana di Ematologia e Oncologia Pediatrica. Haematologica. 2000; 85(4):420-4. PubMedGoogle Scholar
- De Mattia D, Del Vecchio GC, Russo G, De Santis A, Ramenghi U, Notarangelo L, Management of chronic childhood immune thrombocy-topenic purpura: AIEOP consensus guidelines. Acta Haematol. 2010; 123(2):96-109. PubMedhttps://doi.org/10.1159/000268855Google Scholar
- Onaivi ES, Ishiguro H, Gong JP, Patel S, Meozzi PA, Myers L. Functional expression of brain neuronal CB2 cannabinoid receptors are involved in the effects of drugs of abuse and in depression. Ann NY Acad Sci. 2008; 1139:434-49. PubMedhttps://doi.org/10.1196/annals.1432.036Google Scholar
- Rieder SA, Chauhan A, Singh U, Nagarkatti M, Nagarkatti P. Cannabinoid-induced apoptosis in immune cells as a pathway to immunosuppression. Immunobiology. 2010; 215(8):598-605. PubMedhttps://doi.org/10.1016/j.imbio.2009.04.001Google Scholar
- Börner C, Smida M, Höllt V, Schraven B, Kraus J. Cannabinoid receptor type 1- and 2-mediated increase in cyclic AMP inhibits T cell receptor-triggered signaling. J Biol Chem. 2009; 284(51):35450-60. PubMedhttps://doi.org/10.1074/jbc.M109.006338Google Scholar
- Tschop J, Kasten KR, Nogueiras R, Goetzman HS, Cave CM, England LG. The cannabinoid receptor 2 is critical for the host response to sepsis. Immunol. 2009; 183(1):499-505. https://doi.org/10.4049/jimmunol.0900203Google Scholar
- Sipe JC, Arbour N, Gerber A, Beutler E. Reduced endocannabinoid immune modulation by a common cannabinoid 2 (CB2) receptor gene polymorphism: possible risk for autoimmune disorders. J Leukoc Biol. 2005; 78(1):231-8. PubMedhttps://doi.org/10.1189/jlb.0205111Google Scholar