Comprehensive comparison between 222 CTLA-4 haploinsufficiency and 212 LRBA deficiency patients: a systematic review

被引:55
作者
Jamee, M. [1 ,2 ]
Hosseinzadeh, S. [1 ]
Sharifinejad, N. [1 ]
Zaki-Dizaji, M. [3 ]
Matloubi, M. [4 ]
Hasani, M. [5 ]
Baris, S. [6 ]
Alsabbagh, M. [7 ]
Lo, B. [7 ]
Azizi, G. [8 ]
机构
[1] Alborz Univ Med Sci, Student Res Comm, Karaj, Iran
[2] Shahid Beheshti Univ Med Sci, Res Inst Childrens Hlth, Pediat Infect Res Ctr, Tehran, Iran
[3] Legal Med Org, Legal Med Res Ctr, Tehran, Iran
[4] Iran Univ Med Sci, Sch Med, Med Immunol Dept, Tehran, Iran
[5] Alborz Univ Med Sci, CinnaGen Med Biotechnol Res Ctr, Karaj, Iran
[6] Marmara Univ Hosp, Istanbul Jeffrey Modell Diagnost & Res Ctr Primar, Pediat Allergy & Immunol, Istanbul, Turkey
[7] Sidra Med, Div Translat Med, Res Branch, Doha, Qatar
[8] Alborz Univ Med Sci, Non Communicable Dis Res Ctr, Karaj, Iran
关键词
CHAI; CTLA‐ 4; inborn errors of immunity; LATAIE; LRBA; primary immunodeficiency disease;
D O I
10.1111/cei.13600
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytotoxic T lymphocyte antigen 4 (CTLA-4) haploinsufficiency (CHAI) and lipopolysaccharide-responsive beige-like anchor (LRBA) deficiency (LATAIE) are newly identified inborn errors of immunity with shared molecular pathomechanisms and clinical manifestations. In this review, we aimed to provide differential comparisons regarding demographic, clinical, immunological and molecular characteristics between these two similar conditions. A literature search was conducted in PubMed, Web of Science and Scopus databases and included studies were systematically evaluated. Overall, 434 (222 CHAI and 212 LATAIE) patients were found in 101 eligible studies. The CHAI patients were mainly reported from North America and western Europe, while LATAIE patients were predominantly from Asian countries. In CHAI, positive familial history (P < 0 center dot 001) and in LATAIE, consanguineous parents (P < 0 center dot 001) were more common. In CHAI patients the rates of granulomas (P < 0 center dot 001), malignancies (P = 0 center dot 001), atopy (P = 0 center dot 001), cutaneous disorders (P < 0 center dot 001) and neurological (P = 0 center dot 002) disorders were higher, while LATAIE patients were more commonly complicated with life-threatening infections (P = 0 center dot 002), pneumonia (P = 0 center dot 006), ear, nose and throat disorders (P < 0 center dot 001), organomegaly (P = 0 center dot 023), autoimmune enteropathy (P = 0 center dot 038) and growth failure (P < 0 center dot 001). Normal lymphocyte subsets and immunoglobulins except low serum levels of CD9(+) B cells (14 center dot 0 versus 38 center dot 4%, P < 0 center dot 001), natural killer (NK) cells (21 versus 41 center dot 1%, P < 0 center dot 001), immunoglobulin (Ig)G (46 center dot 9 versus 41 center dot 1%, P = 0 center dot 291) and IgA (54 center dot 5 versus 44 center dot 7%, P = 0 center dot 076) were found in the majority of CHAI and LATAIE patients, respectively. The most frequent biological immunosuppressive agents prescribed for CHAI and LATAIE patients were rituximab and abatacept, respectively. Further investigations into the best conditioning and treatment regimens pre- and post-transplantation are required to improve the survival rate of transplanted CHAI and LATAIE patients.
引用
收藏
页码:28 / 43
页数:16
相关论文
共 44 条
[1]   Zero tolerance! A perspective on monogenic disorders with defective regulatory T cells and IBD-like disease [J].
Abdel-Motal, Ussama M. ;
Al-Shaibi, Ahmad ;
Elawad, Mamoun ;
Lo, Bernice .
IMMUNOLOGICAL REVIEWS, 2019, 287 (01) :236-240
[2]   Spectrum of Phenotypes Associated with Mutations in LRBA [J].
Alkhairy, Omar K. ;
Abolhassani, Hassan ;
Rezaei, Nima ;
Fang, Mingyan ;
Andersen, Kasper Krogh ;
Chavoshzadeh, Zahra ;
Mohammadzadeh, Iraj ;
El-Rajab, Mariam A. ;
Massaad, Michel ;
Chou, Janet ;
Aghamohammadi, Asghar ;
Geha, Raif S. ;
Hammarstrom, Lennart .
JOURNAL OF CLINICAL IMMUNOLOGY, 2016, 36 (01) :33-45
[3]   Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation [J].
Alroqi, Fayhan J. ;
Charbonnier, Louis-Marie ;
Baris, Safa ;
Kiykim, Ayca ;
Chou, Janet ;
Platt, Craig D. ;
Algassim, Abdulrahman ;
Keles, Sevgi ;
Al Saud, Bandar K. ;
Alkuraya, Fowzan S. ;
Jordan, Michael ;
Geha, Raif S. ;
Chatila, Talal A. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 141 (03) :1050-+
[4]   Two neurologic facets of CTLA4-related haploinsufficiency [J].
Ayrignac, Xavier ;
Goulabchand, Radjiv ;
Jeziorski, Eric ;
Rullier, Patricia ;
Carra-Dalliere, Clarissa ;
Lozano, Claire ;
Portales, Pierre ;
Vincent, Thierry ;
Viallard, Jean Francois ;
de Champfleur, Nicolas Menjot ;
Rieux-Laucat, Frederic ;
Besnard, Caroline ;
Koenig, Michel ;
Guissart, Claire ;
Labauge, Pierre ;
Guilpain, Philippe .
NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION, 2020, 7 (04)
[5]   Two Faces of LRBA Deficiency in Siblings: Hypogammaglobulinemia and Normal Immunoglobulin Levels [J].
Azizi, G. ;
Abolhassani, H. ;
Habibi, S. ;
Rahamooz, T. ;
Mohammadi, H. ;
Jafarnezhad-Ansariha, F. ;
Mortazavi-jahromi, S. S. ;
Yazdani, R. ;
Aghamohammadi, A. .
JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY, 2018, 28 (01) :48-50
[6]   Polyautoimmunity in Patients with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency [J].
Azizi, Gholamreza ;
Abolhassani, Hassan ;
Zaki-Dizaji, Majid ;
Habibi, Sima ;
Mohammadi, Hamed ;
Shaghaghi, Mohammadreza ;
Yazdani, Reza ;
Anaya, Juan-Manuel ;
Rezaei, Nima ;
Hammarstrom, Lennart ;
Aghamohammadi, Asghar .
IMMUNOLOGICAL INVESTIGATIONS, 2018, 47 (05) :457-467
[7]   Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations [J].
Besnard, Caroline ;
Levy, Eva ;
Aladjidi, Nathalie ;
Stolzenberg, Marie-Claude ;
Magerus-Chatinet, Aude ;
Alibeu, Olivier ;
Nitschke, Patrick ;
Blanche, Stephane ;
Hermine, Olivier ;
Jeziorski, Eric ;
Landman-Parker, Judith ;
Leverger, Guy ;
Mahlaoui, Nizar ;
Michel, Gerard ;
Pellier, Isabelle ;
Suarez, Felipe ;
Thuret, Isabelle ;
de Saint-Basile, Genevieve ;
Picard, Capucine ;
Fischer, Alain ;
Neven, Benedicte ;
Rieux-Laucat, Frederic ;
Quartier, Pierre .
CLINICAL IMMUNOLOGY, 2018, 188 :52-57
[8]   A Spectrum of Clinical Findings from ALPS to CVID: Several Novel LRBA Defects [J].
Cagdas, Deniz ;
Halacli, Sevil Oskay ;
Tan, Cagman ;
Lo, Bernice ;
Cetinkaya, Pinar Gur ;
Esenboga, Saliha ;
Karaatmaca, Betuel ;
Matthews, Helen ;
Balci-Hayta, Burcu ;
Arikoglu, Tuba ;
Ezgu, Fatih ;
Aladag, Elifcan ;
Saltik-Temizel, Inci N. ;
Demir, Huelya ;
Kuskonmaz, Baris ;
Okur, Visal ;
Gumruk, Fatma ;
Goker, Hakan ;
Cetinkaya, Duygu ;
Boztug, Kaan ;
Lenardo, Michael ;
Sanal, Oezden ;
Tezcan, Ilhan .
JOURNAL OF CLINICAL IMMUNOLOGY, 2019, 39 (07) :726-738
[9]   Tregopathies: Monogenic diseases resulting in regulatory T-cell deficiency [J].
Cepika, Alma-Martina ;
Sato, Yohei ;
Liu, Jeffrey Mao-Hwa ;
Uyeda, Molly Javier ;
Bacchetta, Rosa ;
Roncarolo, Maria Grazia .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 142 (06) :1679-1695
[10]   Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center [J].
Crowley, Eileen ;
Warner, Neil ;
Pan, Jie ;
Khalouei, Sam ;
Elkadri, Abdul ;
Fiedler, Karoline ;
Foong, Justin ;
Turinsky, Andrei L. ;
Bronte-Tinkew, Dana ;
Zhang, Shiqi ;
Hu, Jamie ;
Tian, David ;
Li, Dalin ;
Horowitz, Julie ;
Siddiqui, Iram ;
Upton, Julia ;
Roifman, Chaim M. ;
Church, Peter C. ;
Wall, Donna A. ;
Ramani, Arun K. ;
Kotlarz, Daniel ;
Klein, Christoph ;
Uhlig, Holm ;
Snapper, Scott B. ;
Gonzaga-Jauregui, Claudia ;
Paterson, Andrew D. ;
McGovern, Dermot P. B. ;
Brudno, Michael ;
Walters, Thomas D. ;
Griffiths, Anne M. ;
Muise, Aleixo M. .
GASTROENTEROLOGY, 2020, 158 (08) :2208-2220