Identifying immune signatures of common exposures through co-occurrence of T-cell receptors in tens of thousands of donors

Memory T cells are records of clonal expansion from prior immune exposures, such as infections, vaccines and chronic diseases like cancer. A subset of the receptors of these expanded T cells in a typical immune repertoire are highly public, i.e., present in many individuals exposed to the same exposure. For the most part, the exposures associated with these public T cells are unknown. To identify public T-cell receptor signatures of immune exposures, we mined the immunosequencing repertoires of tens of thousands of donors to define clusters of co-occurring T cells. We first built co-occurrence clusters of T cells responding to antigens presented by the same Human Leukocyte Antigen (HLA) and then combined those clusters across HLAs. Each cross-HLA cluster putatively represents the public T-cell signature of a single prevalent exposure. Using repertoires from donors with known serological status for 7 prevalent exposures (HSV-1, HSV-2, EBV, Parvovirus, Toxoplasma gondii , Cytomegalovirus and SARS-CoV-2), we identified a single T-cell cluster strongly associated with each exposure and used it to construct a highly sensitive and specific diagnostic model for the exposure. These T-cell clusters constitute the public immune responses to prevalent exposures, 7 known and many others unknown. By learning the exposure associations for more T-cell clusters, this approach could be used to derive a ledger of a person’s past and present immune exposures. ### Competing Interest Statement DH May, S Woodhouse, R Elyanow, K Doroschak, MT Noakes, R Taniguchi, Z Yang, JR Grino, R Byron, J Oaks, A Sherwood, H Chen-Harris, B Howie and HS Robins have employment and equity ownership with Adaptive Biotechnologies. HJ Zahid and J Greissl have employment and equity ownership with Microsoft Research.