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CD45.1/CD45.2 Congenic Markers Induce a Selective Bias for CD8(+) T Cells during Adoptive Lymphocyte Reconstitution in Lymphocytopenia Mice

CD45.1/CD45.2 congenic markers have been used to track hematopoietic lineage differentiation following hematopoietic stem and progenitor cell (HSPC) transplantation. However, several studies suggest that a bias exists in CD45.1 versus CD45.2 hematopoietic cell reconstitution from HSPCs. Meanwhile, n...

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Detalles Bibliográficos
Autores principales: Kalari Kandy, Rakhee Rathnam, Fan, Xiaoxuan, Cao, Xuefang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AAI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695411/
https://www.ncbi.nlm.nih.gov/pubmed/37938184
http://dx.doi.org/10.4049/immunohorizons.2300014
Descripción
Sumario:CD45.1/CD45.2 congenic markers have been used to track hematopoietic lineage differentiation following hematopoietic stem and progenitor cell (HSPC) transplantation. However, several studies suggest that a bias exists in CD45.1 versus CD45.2 hematopoietic cell reconstitution from HSPCs. Meanwhile, no definitive comparison has been reported for mature immune cells as to whether the CD45.1/CD45.2 disparity can skew the immune cell response. In this study, using lymphocytopenia Rag1(−/−) CD45.2 mice as hosts, we assessed the reconstitution potential of CD45.1 versus CD45.2 lymphocytes following adoptive transfer of mature T and B cells. We have found a selective bias for CD8(+) T cells in that CD45.1 cells showed significantly higher reconstitution compared with CD45.2 cells, whereas CD4(+) T cells and CD19(+) B cells showed equivalent reconstitution. These results suggest that CD45.1/CD45.2 markers may induce an alloreactive response or a survival bias specific to CD8(+) T cells, and they therefore call for caution for using them as congenic markers in immunologic models.