Convergent clonal selection of donor- and recipient-derived CMV-specific T cells in hematopoietic stem cell transplant patients

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 119; no. 6; p. 1
• Main Authors: Erickson, Jami R, Stevens-Ayers, Terry, Mair, Florian, Edmison, Bradley, Boeckh, Michael, Bradley, Philip, Prlic, Martin
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 08.02.2022
• Subjects: Adult; Aged; Aged, 80 and over; Antigens; Biological Sciences; CD8-Positive T-Lymphocytes - immunology; Cell activation; Clonal selection; Competition; Convergence; Cytomegalovirus; Cytomegalovirus - physiology; Cytomegalovirus Infections - immunology; Epitopes; Female; Hematopoietic Stem Cell Transplantation; Hematopoietic stem cells; Humans; Immunodominance; Immunological memory; Lymphocytes; Lymphocytes T; Major histocompatibility complex; Male; Memory cells; Memory T Cells - immunology; Middle Aged; Populations; Stem cell transplantation; Stem cells; T cell receptors; Tissue Donors; Transcriptomics; Virus Activation - immunology; CD8 T cell; T cell competition; CMV reactivation; human transplant
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.2117031119

Competition between antigen-specific T cells for peptide:MHC complexes shapes the ensuing T cell response. Mouse model studies provided compelling evidence that competition is a highly effective mechanism controlling the activation of naïve T cells. However, assessing the effect of T cell competition in the context of a human infection requires defined pathogen kinetics and trackable naïve and memory T cell populations of defined specificity. A unique cohort of nonmyeloablative hematopoietic stem cell transplant patients allowed us to assess T cell competition in response to cytomegalovirus (CMV) reactivation, which was documented with detailed virology data. In our cohort, hematopoietic stem cell transplant donors and recipients were CMV seronegative and positive, respectively, thus providing genetically distinct memory and naïve T cell populations. We used single-cell transcriptomics to track donor versus recipient-derived T cell clones over the course of 90 d. We found that donor-derived T cell clones proliferated and expanded substantially following CMV reactivation. However, for immunodominant CMV epitopes, recipient-derived memory T cells remained the overall dominant population. This dominance was maintained despite more robust clonal expansion of donor-derived T cells in response to CMV reactivation. Interestingly, the donor-derived T cells that were recruited into these immunodominant memory populations shared strikingly similar TCR properties with the recipient-derived memory T cells. This selective recruitment of identical and nearly identical clones from the naïve into the immunodominant memory T cell pool suggests that competition is in place but does not interfere with rejuvenating a memory T cell population. Instead, it results in selection of convergent clones to the memory T cell pool.