• This record comes from PubMed

Recovery of mucosal-associated invariant T cells after myeloablative chemotherapy and autologous peripheral blood stem cell transplantation

. 2016 Nov ; 16 (4) : 529-537. [epub] 20150926

Language English Country Italy Media print-electronic

Document type Journal Article

Links

PubMed 26409838
DOI 10.1007/s10238-015-0384-z
PII: 10.1007/s10238-015-0384-z
Knihovny.cz E-resources

Immune reconstitution after high-dose chemotherapy and stem cell transplantation plays a key role in restoring immunocompetence including defense against infection, immune regulation, and onco-immune surveillance. In this work, we examined the recovery of mucosal-associated invariant T (MAIT) cells, recently discovered innate-like T cells, after various types of myeloablative chemotherapy and autologous peripheral blood stem cell transplantation in 29 patients. We show that MAIT cells are relatively resistant to myeloablative conditioning. The median amount of MAIT cells rises to 43 % around day +30 and is sustained through further measurements on days +60 and +100. Moreover, MAIT cell recovery reaches 100 % of pre-treatment values in 33 % of patients already by day +60. The only factor affecting recovery of MAIT cells is age, younger age being associated with earlier MAIT cell recovery. The pre-treatment quantity of MAIT cells carries a prognostic impact on the early post-transplantation course. Patients with high levels of MAIT cells pre-treatment have significantly lower peak CRP levels (79.45 vs. 150 mg/L) post-treatment, reflecting a clinical trend of less severe infectious complications (less febrile days and less days on intravenous antibiotics). Altogether these data suggest that a high proportion of MAIT cells survive myeloablative chemotherapy and maintain their capacity to fight against infections probably on mucosal surfaces.

See more in PubMed

J Exp Med. 2013 Oct 21;210(11):2305-20 PubMed

Nature. 2012 Nov 29;491(7426):717-23 PubMed

Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):3006-11 PubMed

Proc Natl Acad Sci U S A. 2009 May 19;106(20):8290-5 PubMed

Curr Opin Immunol. 2013 Apr;25(2):174-80 PubMed

Immunity. 2009 Nov 20;31(5):834-44 PubMed

PLoS Biol. 2009 Mar 10;7(3):e54 PubMed

Bone Marrow Transplant. 2005 May;35(9):835-57 PubMed

Scand J Immunol. 2014 Dec;80(6):462-3 PubMed

Intensive Care Med. 2014 Feb;40(2):192-201 PubMed

Nat Immunol. 2010 Aug;11(8):701-8 PubMed

Brain. 2013 Sep;136(Pt 9):2888-903 PubMed

Exp Gerontol. 2014 Jan;49:47-54 PubMed

Scand J Immunol. 2014 Oct;80(4):271-5 PubMed

Blood. 2011 Jan 27;117(4):1250-9 PubMed

Blood. 1997 May 15;89(10):3700-7 PubMed

Bone Marrow Transplant. 1999 Nov;24(10):1079-87 PubMed

J Exp Med. 1999 Jun 21;189(12):1907-21 PubMed

Nature. 2003 Mar 13;422(6928):164-9 PubMed

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...