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CTLA4Ig-primed donor lymphocyte infusions following haploidentical transplantation improve outcome with a distinct pattern of early immune reconstitution as compared to conventional donor lymphocyte infusions in advanced hematological malignancies.
Jaiswal, Sarita Rani; Bhakuni, Prakash; Bhagawati, Gitali; Aiyer, Hema Malini; Soni, Mayank; Sharma, Navneet; Jaiswal, Rishabh Raj; Chakrabarti, Aditi; Chakrabarti, Suparno.
Afiliação
  • Jaiswal SR; Cellular Therapy and Immunology, Manashi Chakrabarti Foundation, Kolkata, India. drsaritaranij@gmail.com.
  • Bhakuni P; Department of Blood and Marrow Transplantation, Dharamshila Narayana Superspeciality Hospital and Research Centre, New Delhi, India. drsaritaranij@gmail.com.
  • Bhagawati G; Cellular Therapy and Immunology, Manashi Chakrabarti Foundation, Kolkata, India.
  • Aiyer HM; Department of Blood and Marrow Transplantation, Dharamshila Narayana Superspeciality Hospital and Research Centre, New Delhi, India.
  • Soni M; Department of Pathology and Microbiology, Dharamshila Narayana Superspeciality Hospital and Research Centre, New Delhi, India.
  • Sharma N; Department of Pathology and Microbiology, Dharamshila Narayana Superspeciality Hospital and Research Centre, New Delhi, India.
  • Jaiswal RR; Department of Blood and Marrow Transplantation, Dharamshila Narayana Superspeciality Hospital and Research Centre, New Delhi, India.
  • Chakrabarti A; Department of Radiology, Dharamshila Narayana Superspeciality Hospital and Research Centre, New Delhi, India.
  • Chakrabarti S; Cellular Therapy and Immunology, Manashi Chakrabarti Foundation, Kolkata, India.
Bone Marrow Transplant ; 56(1): 185-194, 2021 01.
Article em En | MEDLINE | ID: mdl-32704091
ABSTRACT
CTLA4Ig has a unique property to spare or even potentiate natural killer (NK) cell-mediated cytotoxicity, whilst inhibiting T cell activation. We explored the efficacy of prophylactic DLI following CTLA4Ig (CTLA4Ig-DLI group, n = 75), compared to conventional DLI (DLI group, n = 50), in patients with advanced hematological malignancies receiving PTCy-based haploidentical transplantation. Acute and chronic GVHD in the CTLA4Ig-DLI group were 9.6% and 15.3% compared to 18.8% [p = 0.09] and 36.5% [p = 0.01] in the DLI group. Both non-relapse mortality (4% vs 14.4%) and disease progression (DP) (15.7% vs 31.1%) were lower in CTLA4Ig-DLI group (p = 0.04). GVHD and progression-free survival was significantly improved in the CTLA4Ig-DLI group (p = 0.001). The recovery of CD56dimNK cells, NKG2A-KIR + NK subsets and Tregs was significantly better in the CTLA4Ig-DLI group at all time points and memory T cells at day +90. Immune recovery in relation to DP showed distinct patterns, with T cell subsets in the DLI group and NKG2A-KIR+NK cells in CTLA4Ig-DLI group having favorable impact. CTLA4Ig-DLI was thus associated with an improved outcome, possibly on account of the distinct pattern of immune recovery shown with this novel approach.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Neoplasias Hematológicas / Reconstituição Imune / Doença Enxerto-Hospedeiro Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Neoplasias Hematológicas / Reconstituição Imune / Doença Enxerto-Hospedeiro Idioma: En Ano de publicação: 2021 Tipo de documento: Article