Rescigno, The biology of intestinal immunoglobulin A responses, Immunity 28
(2008) 740–750. 2) K. Singh, C. Chang, M.E. Gershwin, IgA deficiency and autoimmunity, Autoimmun. Rev. 13 (2014) 163–177. 3) C.R. Jolliff, K.M. Cost, P.C. Stivrins, P.P. Grossman, C.R. Nolte, S.M. Franco, et al., Reference intervals for serum IgG, IgA, IgM, C3, and C4 as determined by rate nephelometry, Clin. Chem. 28 (1982) 126–128. 4) European Society for Immunodeficiencies, ESID Registry–Working definitions for clinical diagnosis of PID, 2019, Jan 22. https://esid.org/working-parties/registryworking-party-diagnosis- criteria. 5) S. Saghafi, Z. Pourpak, A. Aghamohammadi, A.A. Pourfathollah, A. Samadian, M. Farghadan, et al., Selective immunoglobulin A deficiency in Iranian blood donors: prevalence, laboratory and clinical findings, Iran. J. Allergy, Asthma Immunol. 7 (2008) 157–162. 6) Patel SY, Carbone J, Jolles S (2019): The Expanding Field of Secondary Antibody Deficiency: Causes, Diagnosis, and Management. Front Immunol 10: 33. 7) Na I-K, Buckland M, Agostini C, et al. (2019): Current clinical practice and challenges in the management of secondary immunodeficiency in hematological malignancies. Eur J Haematol 102: 447-456. 8) Benbrahim O, Viallard JF, Choquet S, et al. (2019): The use of octagam and gammanorm in immunodeficiency associated with hematological malignancies: a prospective study from 21 French hematology departments. Hematology 24: 173182. 9) Jahnz-Rozyk K, Roliński J, Siedlar M, et al. (2019): Secondary immunodeficiencies – do we need systemic solutions. JHPOR 1: 2299124. 10) Patel SY, Carbone J, Jolles S (2019): The Expanding Field of Secondary Antibody Deficiency: Causes, Diagnosis, and Management. Front Immunol 10: 33. 11) Na I-K, Buckland M, Agostini C, et al. (2019): Current clini- cal practice and challenges in the management of secondary immunodeficiency in hematological malignancies. Eur J Haematol 102: 447-456. 12) Korzeniowska M, Więsik-Szewczyk E, Jahnz-Różyk K (2018): Opis przypadku chorego na przewlekłą białaczkę limfocytową i ciężkie zapalenie płuc – jak nie przeoczyć wtórnego niedoboru przeciwciał. [Case report of a patient with chronic lymphocytic leukemia and severe pneumonia – how not to miss a secondary antibody deficiency]. Alergologia i Immunologia Współczesna 41: 35-41. 13) Jahnz-Rozyk K, Roliński J, Siedlar M, et al. (2019): Secondary immunodeficiencies – do we need systemic solutions. JHPOR 1: 2299124, https://www.gov.pl/web/zdrowie/programy-lekowe 14) Dhalla F, Misbah SA (2015): Secondary antibody deficiency. Curr Opin Allergy Clin Immunol 15: 505-513. 15) Morrison VA (2010): Infectious complications of chronic lymphocytic leukaemia: pathogenesis, spectrum of infection, preventive approaches. Best Pract Res Clin Haematol 23: 145153. 16) L. Mellemkjaer, L. Hammarstrom, V. Andersen, J. Yuen, C. Heilmann, T. Barington, et al., Cancer risk among patients with IgA deficiency or common variable immunodeficiency and their relatives: a combined Danish and Swedish study, Clin. Exp. Immunol. 130 (2002) 495–500. 17) T. Cheraghi, A. Aghamohammadi, B. Mirminachi, T. Keihanian, E. Hedayat, H. Abolhassani, et al., Prediction of the evolution of common variable immunodeficiency: HLA typing for patients with selective IgA deficiency, J Investig. 18) Puck JM. Newborn screening for severe combined immunodeficiency and T-cell lymphopenia. Immunol Rev. 2019;287(1):241–252. 19) Bonilla FA, Khan DA, Ballas ZK, et al. Practice parameter for the diagnosis and management of primary immunodeficiency. J Allergy Clin Immunol. 2015;136(5). 1186205.e1-78. 20) McAtee CL, Lubega J, Underbrink K, et al. Association of rituximab use with adverse events in children, adolescents, and young adults. JAMA Netw Open. 2021;4(2): e2036321 21) Strehl C, Ehlers L, Gaber T, Buttgereit F. Glucocorticoids-all-rounders tackling the versatile players of the immune system. Front Immunol. 2019;10: 1744. 22) Lodish MB, Keil MF, Stratakis CA. Cushing’s syndrome in pediatrics: an update. Endocrinol Metab Clin North Am. 2018;47(2):451–462. 23) Engel ER, Walter JE. Rituximab and eculizumab when treating nonmalignant hematologic disorders: infection risk, immunization recommendations, and antimicrobial prophylaxis needs. Hematology Am Soc Hematol Educ Program. 2020;1 (1):312–318. 24) McAtee CL, Lubega J, Underbrink K, et al. Association of rituximab use with adverse events in children, adolescents, and young adults. JAMA Netw Open. 2021;4(2): e2036321. 25) Ottaviano G, Marinoni M, Graziani S, et al. Rituximab unveils hypogammaglobulinemia and immunodeficiency in children with autoimmune cytopenia. J Allergy Clin Immunol Pract. 2020;8(1):273–282. 26) Calabrese C, Winthrop KL. Mycobacterial infections potentiated by biologics. Infect Dis Clin North Am. 2020;34(2):413–423. 27) Kaptan Y, Suner A, Tas¸ MN, Oksel F, Aksu K, Sayiner A. Tuberculosis despite latent infection screening and treatment in patients receiving TNF inhibitor therapy. Clin Rheumatol. 2021;40(9):3783–3788. 28) Eom TH, Lee HS, Jang PS, Kim YH. Valproate-induced panhypogammaglobulinemia. Neurol Sci. 2013;34(6):1003–1004 29) M.M. Carneiro-Sampaio, S.B. Carbonare, R.B. Rozentraub, M.N. de Araujo, M.A. Riberiro, M.H. Porto, Frequency of selective IgA deficiency among Brazilian blood donors and healthy pregnant women, Allergol. Immunopathol. 17 (1989) 213–216. 30) L.F. Pereira, A.M. Sapina, J. Arroyo, J. Vinuelas, R.M. Bardaji, L. Prieto, Prevalence of selective IgA deficiency in Spain: more than we thought, Blood 90 (1997) 893. 31) L. Feng, [Epidemiological study of selective IgA deficiency among 6 nationalities in China], Zhonghua Yixue Zazhi 72 (1992), 88-90, 128. 32) T. Kanoh, T. Mizumoto, N. Yasuda, M. Koya, Y. Ohno, H. Uchino, et al., Selective IgA deficiency in Japanese blood donors: frequency and statistical analysis, Vox Sanguinis 50 (1986) 81–86. 33) N. Wang, P. Lu, B. Ling, Z. Zhu, L. Hammarstrom, Caucasian origin of disease associated HLA haplotypes in Chinese blood donors with IgA deficiency, J. Clin.Immunol. 34 (2014) 157–162. 34) J. Koistinen, Familial clustering of selective IgA deficiency, Vox Sanguinis 30 (1976) 181–190 35) M. Frankowiack, R.M. Kovanen, G.A. Repasky, C.K. Lim, C. Song, N.L. Pedersen, et al., The higher frequency of IgA deficiency among Swedish twins is not explained by HLA haplotypes, Genes Immun. 16 (2015) 199–205. 36) R. Yazdani, G. Azizi, H. Abolhassani, A. Aghamohammadi, Selective IgA deficiency: 37) epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and management, Scand. J. Immunol. 85 (2017) 3–12. 38) M.E. Conley, M.D. Cooper, Immature IgA B cells in IgA-deficient patients, N. Engl. J. Med. 305 (1981) 495–497. 39) L. Hammarstrom, B. Lonnqvist, O. Ringden, C.I. Smith, T. Wiebe, Transfer of IgA deficiency to a bone-marrow-grafted patient with aplastic anaemia, Lancet 1 (1985) 778–781. 40) Cunningham-Rundles, Physiology of IgA and IgA deficiency, J. Clin. Immunol. 21 (2001) 303– 309. 41) A.J. Ramsay, A.J. Husband, I.A. Ramshaw, S. Bao, K.I. Matthaei, G. Koehler, et al., The role of interleukin-6 in mucosal IgA antibody responses in vivo, Science 264 (1994) 561–563. 42) S. Borte, Q. Pan-Hammarstrom, C. Liu, U. Sack, M. Borte, U. Wagner, et al., Interleukin-21 restores immunoglobulin production ex vivo in patients with common variable immunode ficiency and selective IgA deficiency, Blood 114 (2009) 4089– 4098. 43) A. Cerutti, The regulation of IgA class switching, Nat. Rev. Immunol. 8 (2008) 421– 434. 44) H. Soheili, H. Abolhassani, N. Arandi, H.A. Khazaei, S. Shahinpour, A. HirbodMobarakeh, et al., Evaluation of natural regulatory T cells in subjects with selective IgA de ficiency: from senior idea to novel opportunities, Int. Arch. Allergy Immunol. 160 (2013) 208– 214. 45) H. Tezuka, T. Ohteki, Regulation of IgA production by intestinal dendritic cells and related cells, Front. Immunol. 10 (2019) 1– 15. 46) J. Ortiz, M. Fernandez-Arquero, E. Urcelay, R. Lopez-Mejias, A. Ferreira, G. Fontan, et al., Interleukin-10 polymorphisms in Spanish IgA de ficiency patients: a casecontrol and family study, BMC Med. Genet. 7 (2006) 56. 47) F.A. Bonilla, D.A. Khan, Z.K. Ballas, J. Chinen, M.M. Frank, J.T. Hsu, et al., Practice parameter for the diagnosis and management of primary immunodeficiency, J. Allergy Clin. Immunol. 136 (2015) 1186–1205, e1-78. 48) R. Yazdani, G. Azizi, H. Abolhassani, A. Aghamohammadi, Selective IgA deficiency: epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and management, Scand. J. Immunol. 85 (2017) 3–12.European Society for Immunodeficiencies, Differential Diagnosis of Hypogammaglobulinemia, 2018. https://ESID.org/education 49) O.H. Robak, M.M. Helmesaat, A.A. Kruglov, S. Prepens, J. Ninnemann, B. Gutbier, et al., Antibiotic treatment-induced secondary IgA deficiency enhances susceptibility to Pseudomonas aeruginosa pneumonia, J. Clin. Investig. 128 (2018) 3535–3545. 50) E.A. Murphy, A.J. Morris, E. Walker, F.D. Lee, R.D. Sturrock, Cyclosporine A induced colitis and acquired selective IgA deficiency in a patient with juvenile chronic arthritis, J. Rheumatol. 20 (1993) 1397–1398. 51) K. Singh, C. Chang, M.E. Gershwin, IgA deficiency and autoimmunity, Autoimmun. Rev. 13 (2014) 163–177. 52) R. Yazdani, A. Latif, F. Tabassomi, H. Abolhassani, G. Aziz, N. Rezaei, et al., Clinical phenotype classification for selective immunoglobulin A deficiency, Expert Rev.Clin. Immunol. 11 (2015) 1245–1254. 53) P. Brandtzaeg, G. Karlsson, G. Hansson, B. Petruson, J. Bjorkander, L.A. Hanson, The clinical condition of IgA-deficient patients is related to the proportion of IgDand IgM-producing cells in their nasal mucosa, Clin. Exp. Immunol. 67 (1987) 626–636. 54) S.G. Sandler, D. Mallory, D. Malamut, R. Eckrich, IgA anaphylactic transfusion reactions, Transfus. Med. Rev. 9 (1995) 1–8. 55) C.J. Ocampo, A.T. Peters, Antibody deficiency in chronic rhinosinusitis: epidemiology and burden of illness, Am. J. Rhinol. Allergy 27 (2013) 34–38. 56) Cunningham-Rundles, Physiology of IgA and IgA deficiency, J. Clin. Immunol. 21 (2001) 303– 309. 57) F.A. Bonilla, D.A. Khan, Z.K. Ballas, J. Chinen, M.M. Frank, J.T. Hsu, et al., Practice parameter for the diagnosis and management of primary immunodeficiency, J. Allergy Clin. Immunol. 136 (2015) 1186–1205, e1-78. 58) M. Janzi, I. Kull, R. Sjoberg, J. Wan, E. Melen, N. Bayat, et al., Selective IgA deficiency in early life: association to infections and allergic diseases during childhood, Clin. Immunol. 133 (2009) 78–85. 59) Edwards, S. Razvi, C. Cunningham-Rundles, IgA deficiency: clinical correlates and responses to pneumococcal vaccine, Clin. Immunol. 111 (2004) 93–97. 60) M.A. French, K.A. Denis, R. Dawkins, J.B. Peter, Severity of infections in IgA deficiency: correlation with decreased serum antibodies to pneumococcal polysaccharides and decreased serum IgG2 and/or IgG4, Clin. Exp. Immunol. 100 (1995) 47–53. 61) H. Ozkan, F. Atlihan, F. Genel, S. Targan, T. Gunvar, IgA and/or IgG subclass deficiency in children with recurrent respiratory infections and its relationship with chronic pulmonary damage, J Investig. Allergol. Clin. Immunol. 15 (2005) 69–74. 62) G.H. Jorgensen, A. Gardulf, M.I. Sigurdsson, S.T. Sigurdardottir, I. Thorsteinsdottir, S. Gudmundsson, et al., Clinical symptoms in adults with selective IgA deficiency: a case-control study, J. Clin. Immunol. 33 (2013) 742–747. 63) Edwards, S. Razvi, C. Cunningham-Rundles, IgA deficiency: clinical correlates and responses to pneumococcal vaccine, Clin. Immunol. 111 (2004) 93–97. 64) B.E. Chipps, R.C. Talamo, J.A. Winkelstein, IgA deficiency, recurrent pneumonias, and bronchiectasis, Chest 73 (1978) 519–526. 65) S. Albin, C. Cunningham-Rundles, An update on the use of immunoglobulin for the treatment of immunodeficiency disorders, Immunotherapy 6 (2014) 1113–1126. 66) S. Zielen, I. Buhring, N. Strnad, J. Reichenbach, D. Hofmann, Immunogenicity and tolerance of a 7-valent pneumococcal conjugate vaccine in nonresponders to the 23valent pneumococcal vaccine, Infect. Immun. 68 (2000) 1435–1440. 67) F.A. Bonilla, D.A. Khan, Z.K. Ballas, J. Chinen, M.M. Frank, J.T. Hsu, et al., Practice parameter for the diagnosis and management of primary immunodeficiency, J. Allergy Clin. Immunol. 136 (2015) 1186–1205, e1-78. 68) H.H. Zinneman, A.P. Kaplan, The association of giardiasis with reduced intestinal secretory immunoglobulin A, Am. J. Dig. Dis. 17 (1972) 793–797. 69) S. Agarwal, L. Mayer, Pathogenesis and treatment of gastrointestinal disease in antibody deficiency syndromes, J. Allergy Clin. Immunol. 124 (2009) 658–664. 70) Norhagen, P.E. Engstrom, L. Hammarstrom, P.O. Soder, C.I. Smith, Immunoglobulin levels in saliva in individuals with selective IgA deficiency: compensatory IgM secretion and its correlation with HLA and susceptibility to infections, J. Clin. Immunol. 9 (1989) 279–286. 71) C. Istrate, J. Hinkula, L. Hammarstrom, L. Svensson, Individuals with selective IgA deficiency resolve rotavirus disease and develop higher antibody titers (IgG, IgG1) than IgA competent individuals, J. Med. Virol. 80 (2008) 531–535. 72) M. Janzi, I. Kull, R. Sjoberg, J. Wan, E. Melen, N. Bayat, et al., Selective IgA deficiency in early life: association to infections and allergic diseases during childhood, Clin. Immunol. 133 (2009) 78–85. A. Aghamohammadi, T. Cheraghi, M. Gharagozlou, M. Movahedi, N. Rezaei, M. Yeganeh, et al., IgA deficiency: correlation between clinical and immunological phenotypes, J. Clin. Immunol. 29 (2009) 130–136. 73) E. Edwards, S. Razvi, C. Cunningham-Rundles, IgA deficiency: clinical correlates and responses to pneumococcal vaccine, Clin. Immunol. 111 (2004) 93–97. 74) A. Franco, R. Parrella, F. Murru, P.R. Ames, F. Martucci, G. Rotiroti, et al., Lack of association between IgA deficiency and respiratory atopy in young male adults, Vivo 25 (2011) 829–832. 75) G.H. Jorgensen, A. Gardulf, M.I. Sigurdsson, S.T. Sigurdardottir, I. Thorsteinsdottir, S. Gudmundsson, et al., Clinical symptoms in adults with selective IgA deficiency: a case-control study, J. Clin. Immunol. 33 (2013) 742–747. 76) C. Cunningham-Rundles, Physiology of IgA and IgA deficiency, J. Clin. Immunol. 21 (2001) 303–309. 77) Abolhassani, B. Gharib, S. Shahinpour, S.N. Masoom, A. Havaei, B. Mirminachi, et al., Autoimmunity in patients with selective IgA deficiency, J Investig. Allergol.Clin. Immunol. 25 (2015) 112–119. 78) K. Singh, C. Chang, M.E. Gershwin, IgA deficiency and autoimmunity, Autoimmun. Rev. 13 (2014) 163–177 79) C. Cunningham-Rundles, W.E. Brandeis, D.J. Pudifin, N.K. Day, R.A. Good, Autoimmunity in selective IgA deficiency: relationship to anti-bovine protein antibodies, circulating immune complexes and clinical disease, Clin. Exp. Immunol.45 (1981) 299–304. 80) J. Mohammadi, R. Ramanujam, S. Jarefors, N. Rezaei, A. Aghamohammadi, P.K. Gregersen, et al., IgA deficiency and the MHC: assessment of relative risk and microheterogeneity within the HLA A1 B8, DR3 (8.1) haplotype, J. Clin. Immunol.30 (2010) 138–143. 81) Soheili, H. Abolhassani, N. Arandi, H.A. Khazaei, S. Shahinpour, A. HirbodMobarakeh, et al., Evaluation of natural regulatory T cells in subjects with selective IgA de ficiency: from senior idea to novel opportunities, Int. Arch. Allergy Immunol. 160 (2013) 208– 214. 82) E. Gianchecchi, D.V. Delfino, A. Fierabracci, NK cells in autoimmune diseases: linking innate and adaptive immune responses, Autoimmun. Rev. 17 (2018) 142–154. 83) M. Cattalini, M. Soliani, M.C. Caparello, R. Cimaz, Sex differences in pediatric rheumatology, Clin. Rev. Allergy Immunol. 56 (2019) 293–307. 84) R.C. Ferreira, Q. Pan-Hammarstrom, R.R. Graham, V. Gateva, G. Fontan, A.T. Lee, et al., Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency, Nat. Genet. 42 (2010) 777–780. 85) R.C. Ferreira, Q. Pan-Hammarstrom, R.R. Graham, V. Gateva, G. Fontan, A.T. Lee, et al., Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency, Nat. Genet. 42 (2010) 777–780. 86) M.A. Heneghan, F.M. Stevens, E.M. Cryn, et al., Celiac sprue and immunodeficiency states: a 25 year review, J. Clin. Gasteroentrol 25 (1997) 421–425. 87) V. Lougaris, A. Sorlini, C. Monfredini, G. Ingrasciotta, A. Caravaggio, T. Lorenzini, et al., Clinical and laboratory features of 184 Italian pediatric patients affected with selective IgA deficiency (SIgAD): a longitudinal single-center study, J. Clin.Immunol. 39 (2019) 470–475. 88) R. Yazdani, G. Azizi, H. Abolhassani, A. Aghamohammadi, Selective IgA deficiency: 89) epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and management, Scand. J. Immunol. 85 (2017) 3–12. 90) M.A. Chow, B. Lebwohl, N.R. Reilly, P.H. Green, Immunoglobulin A deficiency in celiac disease, J. Clin. Gastroenterol. 46 (2012) 850–854. 91) 1.Yazdani R, Azizi G, Abolhassani H, Aghamohammadi A. Selective IgA Deficiency: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management. Scand J Immunol. 2017 Jan;85(1):3-12. [PubMed] 92) Mertin S, Thomson I. What you need to know about IgA deficiency: a case study. J Am Assoc Nurse Pract. 2014 May;26(5):268-72. [PubMed] 93) Patel SY, Carbone J, Jolles S. The Expanding Field of Secondary Antibody Deficiency: Causes, Diagnosis, and Management. Front Immunol. 2019;10:33. [PMC free article] [PubMed] 94) Singh K, Chang C, Gershwin ME. IgA deficiency and autoimmunity. Autoimmun Rev. 2014 Feb;13(2):163-77. [PubMed] 95) Murphy EA, Morris AJ, Walker E, Lee FD, Sturrock RD. Cyclosporine A induced colitis and acquired selective IgA deficiency in a patient with juvenile chronic arthritis. J Rheumatol. 1993 Aug;20(8):1397-8. [PubMed] 96) Aarli JA. Drug-induced IgA deficiency in epileptic patients. Arch Neurol. 1976 Apr;33(4):296-9. [PubMed] 97) Snowden N, Dietch DM, Teh LS, Hilton RC, Haeney MR. Antibody deficiency associated with gold treatment: natural history and management in 22 patients. Ann Rheum Dis. 1996 Sep;55(9):616-21. [PMC free article] [PubMed] 98) Hjalmarson O, Hanson LA, Nilsson LA. IgA deficiency during D-penicillamine treatment. Br Med J. 1977 Feb 26;1(6060):549. [PMC free article] [PubMed] 99) Vo Ngoc DT, Krist L, van Overveld FJ, Rijkers GT. The long and winding road to IgA deficiency: causes and consequences. Expert Rev Clin Immunol. 2017 Apr;13(4):371-382. [PubMed] 100) Woof JM, Kerr MA. The function of immunoglobulin A in immunity. J Pathol. 2006 Jan;208(2):270-82. [PubMed] 101) Hammarström L, Vorechovsky I, Webster D. Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID). Clin Exp Immunol. 2000 May;120(2):225-31. [PMC free article] [PubMed] 102) Swain S, Selmi C, Gershwin ME, Teuber SS. The clinical implications of selective IgA deficiency. J Transl Autoimmun. 2019 Dec;2:100025. [PMC free article] [PubMed] 103) Cunningham-Rundles C. Physiology of IgA and IgA deficiency. J Clin Immunol. 2001 Sep;21(5):303-9. [PubMed] 104) Kaplan B, Kopyltsova Y, Khokhar A, Lam F, Bonagura V. Rituximab and immune deficiency: case series and review of the literature. J Allergy Clin Immunol Pract. 2014 Sep- Oct;2(5):594-600. [PubMed] 105) Lycke N, Erlandsson L, Ekman L, Schön K, Leanderson T. Lack of J chain inhibits the transport of gut IgA and abrogates the development of intestinal antitoxic protection. J Immunol. 1999 Jul 15;163(2):913-9. [PubMed] 106) Johansen FE, Braathen R, Brandtzaeg P. Role of J chain in secretory immunoglobulin formation. Scand J Immunol. 2000 Sep;52(3):240-8. [PubMed] 107) Mella MA, Lavrinienko A, Akhi R, Hindström R, Nissinen AE, Wang C, Kullaa A, Salo T, Auvinen J, Koskimäki JJ, Hörkkö S. Compensatory IgM to the Rescue: Patients with Selective IgA Deficiency Have Increased Natural IgM Antibodies to MAA-LDL and No Changes in Oral Microbiota. Immunohorizons. 2021 Apr 23;5(4):170-181. [PubMed] 108) Aghamohammadi A, Abolhassani H, Biglari M, Abolmaali S, Moazzami K, Tabatabaeiyan M, Asgarian-Omran H, Parvaneh N, Mirahmadian M, Rezaei N. Analysis of switched memory B cells in patients with IgA deficiency. Int Arch Allergy Immunol. 2011;156(4):462-8. [PubMed] 109) Abolhassani H, Aghamohammadi A, Hammarström L. Monogenic mutations associated with IgA deficiency. Expert Rev Clin Immunol. 2016 Dec;12(12):1321-1335. [PubMed] 110) Giza S, Kotanidou E, Papadopoulou-Alataki E, Antoniou MC, Maggana I, Kyrgios I, Galli-Tsinopoulou A. Prevalence of selective immunoglobulin A deficiency in Greek children and adolescents with type 1 diabetes. World J Pediatr. 2016 Nov;12(4):470-476. [PubMed] 111) Gulez N, Karaca NE, Aksu G, Kutukculer N. Increased percentages of autoantibodies in immunoglobulin A-deficient children do not correlate with clinical manifestations. Autoimmunity. 2009 Jan;42(1):74-9. [PubMed] 112) Méndez Loayza DLÁ, Arriola Spátola MA, Gonzáles de Campos AL, Montenegro Pucci C, Olano Gossweiler C. [Prevalence and characteristics of selective IgA deficiency in celiac patients]. Rev Gastroenterol Peru. 2021 Jan-Mar;41(1):11-15. [PubMed] 113) Qamar N, Fuleihan RL. The hyper IgM syndromes. Clin Rev Allergy Immunol. 2014 Apr;46(2):120-30. [PubMed] 114) Agarwal S, Cunningham-Rundles C. Thymoma and immunodeficiency (Good syndrome): a report of 2 unusual cases and review of the literature. Ann Allergy Asthma Immunol. 2007 Feb;98(2):185-90. [PMC free article] [PubMed] 115) Sørrig R, Klausen TW, Salomo M, Vangsted AJ, Frølund UC, Andersen KT, Klostergaard A, Helleberg C, Pedersen RS, Pedersen PT, Helm-Petersen S, Teodorescu EM, Preiss B, Abildgaard N, Gimsing P., Danish Myeloma Study Group. Immunoparesis in newly diagnosed Multiple Myeloma patients: Effects on overall survival and progression free survival in the Danish population. PLoS One. 2017;12(12):e0188988. [PMC free article] [PubMed] 116) Ozkan H, Atlihan F, Genel F, Targan S, Gunvar T. IgA and/or IgG subclass deficiency in children with recurrent respiratory infections and its relationship with chronic pulmonary damage. J Investig Allergol Clin Immunol. 2005;15(1):69-74. [PubMed] 117) Schussler E, Beasley MB, Maglione PJ. Lung Disease in Primary Antibody Deficiencies. J Allergy Clin Immunol Pract. 2016 Nov - Dec;4(6):1039-1052. [PMC free article] [PubMed] 118) Ludvigsson JF, Neovius M, Ye W, Hammarström L. IgA deficiency and risk of cancer: a population-based matched cohort study. J Clin Immunol. 2015 Feb;35(2):182-8. [PubMed] 119) Quiding-Järbrink M, Sundström P, Lundgren A, Hansson M, Bäckström M, Johansson C, Enarsson K, Hermansson M, Johnsson E, Svennerholm AM. Decreased IgA antibody production in the stomach of gastric adenocarcinoma patients. Clin Immunol. 2009 Jun;131(3):463-71. [PubMed] 120) Mathew SK, Anjum F. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Jun 19, 2022. Transfusion Selective IgA Deficiency. [PubMed] 121) Çölkesen F, Kandemir B, Arslan Ş, Çölkesen F, Yıldız E, Korkmaz C, Vatansev H, Evcen R, Aykan FS, Kılınç M, Aytekin G, Feyzioğlu B, Doğan M, Teke T. Relationship between Selective IgA Deficiency and COVID-19 Prognosis. Jpn J Infect Dis. 2022 May 24;75(3):228- 233. [PubMed] 122) Quinti I, Mortari EP, Fernandez Salinas A, Milito C, Carsetti R. IgA Antibodies and IgA Deficiency in SARS-CoV-2 Infection. Front Cell Infect Microbiol. 2021;11:655896. [PMC free article] [PubMed]