Defining HPV-specific B cell responses in patients with head and neck cancer

Article

关键词: TERTIARY LYMPHOID STRUCTURES;    HUMAN-PAPILLOMAVIRUS;    PLASMA-CELLS;    SERUM ANTIBODIES;    IMMUNOTHERAPY;    SURVIVAL;    LYMPHOCYTES;    EXPRESSION;    BLOOD;   

DOI  :  10.1038/s41586-020-2931-3

来源: SCIE

【 摘 要 】

Detailed analyses of B cells in the tumour microenvironment of human papilloma virus (HPV)-linked head and neck cancers reveal strong humoral immune responses to HPV antigens and the secretion of HPV-specific antibodies in situ. Tumours often contain B cells and plasma cells but the antigen specificity of these intratumoral B cells is not well understood(1-8). Here we show that human papillomavirus (HPV)-specific B cell responses are detectable in samples from patients with HPV-positive head and neck cancers, with active production of HPV-specific IgG antibodies in situ. HPV-specific antibody secreting cells (ASCs) were present in the tumour microenvironment, with minimal bystander recruitment of influenza-specific cells, suggesting a localized and antigen-specific ASC response. HPV-specific ASC responses correlated with titres of plasma IgG and were directed against the HPV proteins E2, E6 and E7, with the most dominant response against E2. Using intratumoral B cells and plasma cells, we generated several HPV-specific human monoclonal antibodies, which exhibited a high degree of somatic hypermutation, consistent with chronic antigen exposure. Single-cell RNA sequencing analyses detected activated B cells, germinal centre B cells and ASCs within the tumour microenvironment. Compared with the tumour parenchyma, B cells and ASCs were preferentially localized in the tumour stroma, with well-formed clusters of activated B cells indicating ongoing germinal centre reactions. Overall, we show that antigen-specific activated and germinal centre B cells as well as plasma cells can be found in the tumour microenvironment. Our findings provide a better understanding of humoral immune responses in human cancer and suggest that tumour-infiltrating B cells could be harnessed for the development of therapeutic agents.

【 授权许可】

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