DataSheet_1_CD8+ T-Cell Repertoire in Human Leukocyte Antigen Class I-Mismatched Alloreactive Immune Response.docx

التفاصيل البيبلوغرافية
العنوان: DataSheet_1_CD8+ T-Cell Repertoire in Human Leukocyte Antigen Class I-Mismatched Alloreactive Immune Response.docx
المؤلفون: Florence Bettens (7877345), Zuleika Calderin Sollet (10008968), Stéphane Buhler (149592), Jean Villard (41257)
سنة النشر: 2021
المجموعة: Smithsonian Institution: Digital Repository
مصطلحات موضوعية: Immunology, Applied Immunology (incl. Antibody Engineering, Xenotransplantation and T-cell Therapies), Autoimmunity, Cellular Immunology, Humoural Immunology and Immunochemistry, Immunogenetics (incl. Genetic Immunology), Innate Immunity, Transplantation Immunology, Tumour Immunology, Immunology not elsewhere classified, Genetic Immunology, Animal Immunology, Veterinary Immunology, T-cell alloreactivity, human leukocyte antigen (HLA), T-cell repertoire, T-cell receptor, hematopoietic stem cell transplantation (HSCT)
الوصف: In transplantation, direct allorecognition is a complex interplay between T-cell receptors (TCR) and HLA molecules and their bound peptides expressed on antigen-presenting cells. In analogy to HLA mismatched hematopoietic stem cell transplantation (HSCT), the TCR CDR3β repertoires of alloreactive cytotoxic CD8 + responder T cells, defined by the cell surface expression of CD137 and triggered in vitro by HLA mismatched stimulating cells, were analyzed in different HLA class I mismatched combinations. The same HLA mismatched stimulatory cells induced very different repertoires in distinct but HLA identical responders. Likewise, stimulator cells derived from HLA identical donors activated CD8 + cells expressing very different repertoires in the same mismatched responder. To mimic in vivo inflammation, expression of HLA class l antigens was upregulated in vitro on stimulating cells by the inflammatory cytokines TNFα and IFNβ. The repertoires differed whether the same responder cells were stimulated with cells treated or not with both cytokines. In conclusion, the selection and expansion of alloreactive cytotoxic T-cell clonotypes expressing a very diverse repertoire is observed repeatedly despite controlling for HLA disparities and is significantly influenced by the inflammatory status. This makes prediction of alloreactive T-cell repertoires a major challenge in HLA mismatched HSCT.
نوع الوثيقة: dataset
اللغة: unknown
Relation: https://figshare.com/articles/dataset/DataSheet_1_CD8_T-Cell_Repertoire_in_Human_Leukocyte_Antigen_Class_I-Mismatched_Alloreactive_Immune_Response_docx/13613876
DOI: 10.3389/fimmu.2020.588741.s001
الاتاحة: https://doi.org/10.3389/fimmu.2020.588741.s001
Rights: CC BY 4.0
رقم الانضمام: edsbas.CC459FD2
قاعدة البيانات: BASE
الوصف
DOI:10.3389/fimmu.2020.588741.s001