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.
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。