Helper T cell immunity in humans with inherited CD4 deficiency.

IF 12.6 1区 医学 Q1 IMMUNOLOGY Journal of Experimental Medicine Pub Date : 2024-05-06 Epub Date: 2024-04-01 DOI:10.1084/jem.20231044
Antoine Guérin, Marcela Moncada-Vélez, Katherine Jackson, Masato Ogishi, Jérémie Rosain, Mathieu Mancini, David Langlais, Andrea Nunez, Samantha Webster, Jesse Goyette, Taushif Khan, Nico Marr, Danielle T Avery, Geetha Rao, Tim Waterboer, Birgitta Michels, Esmeralda Neves, Cátia Iracema Morais, Jonathan London, Stéphanie Mestrallet, Pierre Quartier Dit Maire, Bénédicte Neven, Franck Rapaport, Yoann Seeleuthner, Atar Lev, Amos J Simon, Jorge Montoya, Ortal Barel, Julio Gómez-Rodríguez, Julio C Orrego, Anne-Sophie L'Honneur, Camille Soudée, Jessica Rojas, Alejandra C Velez, Irini Sereti, Benjamin Terrier, Nancy Marin, Luis F García, Laurent Abel, Stéphanie Boisson-Dupuis, Joel Reis, Antonio Marinho, Andrea Lisco, Emilia Faria, Christopher C Goodnow, Julia Vasconcelos, Vivien Béziat, Cindy S Ma, Raz Somech, Jean-Laurent Casanova, Jacinta Bustamante, Jose Luis Franco, Stuart G Tangye
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Abstract

CD4+ T cells are vital for host defense and immune regulation. However, the fundamental role of CD4 itself remains enigmatic. We report seven patients aged 5-61 years from five families of four ancestries with autosomal recessive CD4 deficiency and a range of infections, including recalcitrant warts and Whipple's disease. All patients are homozygous for rare deleterious CD4 variants impacting expression of the canonical CD4 isoform. A shorter expressed isoform that interacts with LCK, but not HLA class II, is affected by only one variant. All patients lack CD4+ T cells and have increased numbers of TCRαβ+CD4-CD8- T cells, which phenotypically and transcriptionally resemble conventional Th cells. Finally, patient CD4-CD8- αβ T cells exhibit intact responses to HLA class II-restricted antigens and promote B cell differentiation in vitro. Thus, compensatory development of Th cells enables patients with inherited CD4 deficiency to acquire effective cellular and humoral immunity against an unexpectedly large range of pathogens. Nevertheless, CD4 is indispensable for protective immunity against at least human papillomaviruses and Trophyrema whipplei.

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遗传性 CD4 缺乏症患者的辅助性 T 细胞免疫。
CD4+ T 细胞对宿主防御和免疫调节至关重要。然而,CD4本身的基本作用仍然是个谜。我们报告了来自四个血统的五个家庭的七名 5-61 岁患者,他们都患有常染色体隐性 CD4 缺乏症和一系列感染,包括顽固性尖锐湿疣和惠普尔病。所有患者都是影响CD4同工酶表达的罕见CD4有害变异基因的同卵双生者。一种表达较短的异构体仅受一个变异体的影响,该异构体与 LCK 相互作用,但与 HLA II 类无关。所有患者都缺乏 CD4+ T 细胞,而 TCRαβ+CD4-CD8- T 细胞数量增加,这些细胞在表型和转录上与传统 Th 细胞相似。最后,患者的 CD4-CD8- αβ T 细胞对 HLA II 类限制性抗原表现出完整的反应,并在体外促进 B 细胞分化。因此,Th 细胞的代偿性发育能使遗传性 CD4 缺乏症患者获得有效的细胞免疫和体液免疫,以抵抗大量病原体。尽管如此,CD4 至少对人类乳头状瘤病毒和白喉杆菌的保护性免疫是不可或缺的。
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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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