靶向分枝杆菌转运蛋白的人源抗体可介导对结核病的保护。
Human antibodies targeting a Mycobacterium transporter protein mediate protection against tuberculosis.
机构信息
Department of Clinical Microbiology and Immunology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
Centre for Global Health and Infectious Diseases, Collaborative Innovation Centre for the Diagnosis and Treatment of Infectious Diseases, Tsinghua University School of Medicine, Beijing, China.
出版信息
Nat Commun. 2021 Jan 27;12(1):602. doi: 10.1038/s41467-021-20930-0.
Mycobacterium tuberculosis (Mtb) exposure drives antibody responses, but whether patients with active tuberculosis elicit protective antibodies, and against which antigens, is still unclear. Here we generate monoclonal antibodies from memory B cells of one patient to investigate the B cell responses during active infection. The antibodies, members of four distinct B cell clones, are directed against the Mtb phosphate transporter subunit PstS1. Antibodies p4-36 and p4-163 reduce Mycobacterium bovis-BCG and Mtb levels in an ex vivo human whole blood growth inhibition assay in an FcR-dependent manner; meanwhile, germline versions of p4-36 and p4-163 do not bind Mtb. Crystal structures of p4-36 and p4-170, complexed to PstS1, are determined at 2.1 Å and 2.4 Å resolution, respectively, to reveal two distinctive PstS1 epitopes. Lastly, a prophylactic p4-36 and p4-163 treatment in Mtb-infected Balb/c mice reduces bacterial lung burden by 50%. Our study shows that inhibitory anti-PstS1 B cell responses arise during active tuberculosis.
结核分枝杆菌(Mtb)暴露会引发抗体反应,但活动性肺结核患者是否会产生保护性抗体,以及针对哪些抗原,目前仍不清楚。在这里,我们从一名患者的记忆 B 细胞中产生了单克隆抗体,以研究活动性感染期间的 B 细胞反应。这些抗体是四个不同 B 细胞克隆的成员,针对 Mtb 磷酸盐转运体亚基 PstS1。抗体 p4-36 和 p4-163 以 FcR 依赖的方式减少了牛分枝杆菌卡介苗和 Mtb 在体外人全血生长抑制测定中的水平;同时,p4-36 和 p4-163 的种系版本不与 Mtb 结合。p4-36 和 p4-170 与 PstS1 复合物的晶体结构分别以 2.1Å 和 2.4Å 的分辨率确定,以揭示两个独特的 PstS1 表位。最后,预防性给予 p4-36 和 p4-163 治疗感染 Mtb 的 Balb/c 小鼠可使肺部细菌负荷减少 50%。我们的研究表明,在活动性肺结核期间会产生抑制性抗 PstS1 B 细胞反应。