Academic Journal

Mass cytometry reveals immune signatures associated with cytomegalovirus (CMV) control in recipients of allogeneic haemopoietic stem cell transplant and CMV‐specific T cells

التفاصيل البيبلوغرافية
العنوان: Mass cytometry reveals immune signatures associated with cytomegalovirus (CMV) control in recipients of allogeneic haemopoietic stem cell transplant and CMV‐specific T cells
المؤلفون: Helen M McGuire, Simone Rizzetto, Barbara P Withers, Leighton E Clancy, Selmir Avdic, Lauren Stern, Ellis Patrick, Barbara Fazekas de St Groth, Barry Slobedman, David J Gottlieb, Fabio Luciani, Emily Blyth
المصدر: Clinical & Translational Immunology, Vol 9, Iss 7, Pp n/a-n/a (2020)
بيانات النشر: Wiley, 2020.
سنة النشر: 2020
المجموعة: LCC:Immunologic diseases. Allergy
مصطلحات موضوعية: adoptive T‐cell therapy, CyTOF, haemopoietic stem cell transplant, immune reconstitution, immunotherapy, mass cytometry, Immunologic diseases. Allergy, RC581-607
الوصف: Abstract Objectives Cytomegalovirus (CMV) is known to have a significant impact on immune recovery post‐allogeneic haemopoietic stem cell transplant (HSCT). Adoptive therapy with donor‐derived or third‐party virus‐specific T cells (VST) can restore CMV immunity leading to clinical benefit in prevention and treatment of post‐HSCT infection. We developed a mass cytometry approach to study natural immune recovery post‐HSCT and assess the mechanisms underlying the clinical benefits observed in recipients of VST. Methods A mass cytometry panel of 38 antibodies was utilised for global immune assessment (72 canonical innate and adaptive immune subsets) in HSCT recipients undergoing natural post‐HSCT recovery (n = 13) and HSCT recipients who received third‐party donor‐derived CMV‐VST as salvage for unresponsive CMV reactivation (n = 8). Results Mass cytometry identified distinct immune signatures associated with CMV characterised by a predominance of innate cells (monocytes and NK) seen early and an adaptive signature with activated CD8+ T cells seen later. All CMV‐VST recipients had failed standard antiviral pharmacotherapy as a criterion for trial involvement; 5/8 had failed to develop the adaptive immune signature by study enrolment despite significant CMV antigen exposure. Of these, VST administration resulted in development of the adaptive signature in association with CMV control in three patients. Failure to respond to CMV‐VST in one patient was associated with persistent absence of the adaptive immune signature. Conclusion The clinical benefit of CMV‐VST may be mediated by the recovery of an adaptive immune signature characterised by activated CD8+ T cells.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2050-0068
Relation: https://doaj.org/toc/2050-0068
DOI: 10.1002/cti2.1149
URL الوصول: https://doaj.org/article/384c8880cd844db5ba2efffe167bcaae
رقم الانضمام: edsdoj.384c8880cd844db5ba2efffe167bcaae
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20500068
DOI:10.1002/cti2.1149