人类遗传性 CD4 缺陷中的辅助性 T 细胞免疫。
Helper T cell immunity in humans with inherited CD4 deficiency.
机构信息
Garvan Institute of Medical Research , Darlinghurst, Australia.
Faculty of Medicine and Health, School of Clinical Medicine, University of New South Wales Sydney, Sydney, Australia.
出版信息
J Exp Med. 2024 May 6;221(5). doi: 10.1084/jem.20231044. Epub 2024 Apr 1.
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.
CD4+ T 细胞对于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。我们报告了来自五个家族的七名患者,他们的年龄在 5 至 61 岁之间,具有常染色体隐性 CD4 缺乏症和一系列感染,包括顽固的疣和 Whipple 病。所有患者均为纯合子,携带有影响典型 CD4 同种型表达的罕见有害 CD4 变体。一种较短的表达同种型与 LCK 相互作用,但不与 HLA Ⅱ类相互作用,仅受一种变体影响。所有患者均缺乏 CD4+ T 细胞,并且 TCRαβ+CD4-CD8- T 细胞数量增加,这些细胞在表型和转录上类似于常规 Th 细胞。最后,患者的 CD4-CD8- αβ T 细胞对 HLA Ⅱ类限制的抗原表现出完整的反应,并在体外促进 B 细胞分化。因此,Th 细胞的代偿性发育使患有遗传性 CD4 缺乏症的患者能够获得针对范围广泛的病原体的有效细胞和体液免疫。然而,CD4 对于针对至少人乳头瘤病毒和 Trophyrema whipplei 的保护性免疫是必不可少的。