种系变异和镶嵌染色体改变影响COVID-19疫苗的免疫原性。

IF 11.1 Q1 CELL BIOLOGY
Cell genomics Pub Date : 2025-03-12 Epub Date: 2025-03-04 DOI:10.1016/j.xgen.2025.100783
Kyuto Sonehara, Yoshifumi Uwamino, Ryunosuke Saiki, Masaru Takeshita, Shinichi Namba, Shunsuke Uno, Tomoko Nakanishi, Tomoyasu Nishimura, Tatsuhiko Naito, Go Sato, Masahiro Kanai, Aoxing Liu, Sho Uchida, Toshinobu Kurafuji, Akiko Tanabe, Tomoko Arai, Akemi Ohno, Ayako Shibata, Shiho Tanaka, Masatoshi Wakui, Shoko Kashimura, Chiharu Tomi, Akemi Hara, Shiori Yoshikawa, Keiko Gotanda, Kana Misawa, Hiromu Tanaka, Shuhei Azekawa, Qingbo S Wang, Ryuya Edahiro, Yuya Shirai, Kenichi Yamamoto, Genta Nagao, Takuo Suzuki, Masato Kiyoshi, Akiko Ishii-Watabe, Shinichi Higashiue, Shuzo Kobayashi, Hiroki Yamaguchi, Yasushi Okazaki, Naoyuki Matsumoto, Akihide Masumoto, Hidenobu Koga, Akinori Kanai, Yoshiya Oda, Yutaka Suzuki, Koichi Matsuda, Yuko Kitagawa, Ryuji Koike, Akinori Kimura, Atsushi Kumanogoh, Akihiko Yoshimura, Seiya Imoto, Satoru Miyano, Takanori Kanai, Koichi Fukunaga, Naoki Hasegawa, Mitsuru Murata, Hiromichi Matsushita, Seishi Ogawa, Yukinori Okada, Ho Namkoong
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引用次数: 0

摘要

疫苗的免疫原性受接种者遗传背景的影响。在这里,我们对1559名日本血统的mRNA-1273和537名BNT162b2疫苗接种者进行了疫苗诱导的sars - cov -2特异性免疫球蛋白G (IgG)抗体滴度和T细胞免疫反应的全基因组关联研究。sars - cov -2特异性抗体滴度与免疫球蛋白重链(IGH)和主要组织相容性复合体(MHC)位点相关,T细胞反应与MHC相关。IGH的先导变异包含一个群体特异性错义变异(rs1043109-C;p.Leu192Val)在免疫球蛋白重常数γ 1基因(IGHG1)中的表达,具有较强的降低作用(β = -0.54)。抗体滴度相关的变异调节循环免疫调节蛋白(例如,LILRB4和FCRL6)。年龄相关的造血扩展马赛克染色体改变(mCAs)影响MHC和IGH也损害抗体的产生。影响MHC-/ igh的mca会导致感染性和免疫性疾病风险,包括败血症和格雷夫斯病。研究了X/Y染色体扩展的镶嵌损失对这些表型的影响。总之,生殖系和体细胞突变都有助于适应性免疫功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Germline variants and mosaic chromosomal alterations affect COVID-19 vaccine immunogenicity.

Vaccine immunogenicity is influenced by the vaccinee's genetic background. Here, we perform a genome-wide association study of vaccine-induced SARS-CoV-2-specific immunoglobulin G (IgG) antibody titers and T cell immune responses in 1,559 mRNA-1273 and 537 BNT162b2 vaccinees of Japanese ancestry. SARS-CoV-2-specific antibody titers are associated with the immunoglobulin heavy chain (IGH) and major histocompatibility complex (MHC) locus, and T cell responses are associated with MHC. The lead variants at IGH contain a population-specific missense variant (rs1043109-C; p.Leu192Val) in the immunoglobulin heavy constant gamma 1 gene (IGHG1), with a strong decreasing effect (β = -0.54). Antibody-titer-associated variants modulate circulating immune regulatory proteins (e.g., LILRB4 and FCRL6). Age-related hematopoietic expanded mosaic chromosomal alterations (mCAs) affecting MHC and IGH also impair antibody production. MHC-/IGH-affecting mCAs confer infectious and immune disease risk, including sepsis and Graves' disease. Impacts of expanded mosaic loss of chromosomes X/Y on these phenotypes were examined. Altogether, both germline and somatic mutations contribute to adaptive immunity functions.

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