Literature DB >> 33420393

Reduced leukemia relapse through cytomegalovirus reactivation in killer cell immunoglobulin-like receptor-ligand-mismatched cord blood transplantation.

Hisayuki Yokoyama1, Junya Kanda2, Yuta Kawahara3, Naoyuki Uchida4, Masatsugu Tanaka5, Satoshi Takahashi6, Makoto Onizuka7, Yuma Noguchi8, Yukiyasu Ozawa9, Yuna Katsuoka10, Shuichi Ota11, Takanori Ohta12, Takafumi Kimura13, Yoshinobu Kanda14, Tatsuo Ichinohe15, Yoshiko Atsuta16,17, Hideki Nakasone18, Satoko Morishima19.   

Abstract

Cytomegalovirus (CMV) reactivation in cord blood transplantation (CBT) may result in the proliferation and maturation of natural killer (NK) cells. Similarly, a mismatch of the killer cell immunoglobulin-like receptor (KIR)-ligand induces NK cell activation. Therefore, if CMV reactivation occurs in the presence of KIR-ligand mismatch, it might improve CBT outcomes. We assessed the difference in the effect of CMV reactivation in the presence of KIR-ligand mismatch on disease relapse in the graft-versus-host direction. A total of 2840 patients with acute myeloid leukemia, acute lymphoblastic leukemia, myelodysplastic syndrome, and chronic myeloid leukemia were analyzed. Among those with a HLA-Bw4/A3/A11 (KIR3DL-ligand) mismatch, CMV reactivation up to 100 days following CBT had a favorable impact on relapse (18.9% vs. 32.9%, P = 0.0149). However, this effect was not observed in cases without the KIR3DL-ligand mismatch or in those with or without a HLA-C1/C2 (KIR2DL-ligand) mismatch. The multivariate analysis suggested that CMV reactivation had a favorable effect on relapse only in cases with a KIR3DL-ligand mismatch (hazard ratio 0.54, P = 0.032). Moreover, the interaction effect between CMV reactivation and KIR3DL-ligand mismatch on relapse was significant (P = 0.039). Thus, our study reveals the association between KIR-ligand mismatches and CMV reactivation, which will enhance CBT outcomes.

Entities:  

Year:  2021        PMID: 33420393     DOI: 10.1038/s41409-020-01203-8

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN: 0268-3369            Impact factor:   5.483


  33 in total

1.  Cytomegalovirus reactivation after allogeneic transplantation promotes a lasting increase in educated NKG2C+ natural killer cells with potent function.

Authors:  Bree Foley; Sarah Cooley; Michael R Verneris; Michelle Pitt; Julie Curtsinger; Xianghua Luo; Sandra Lopez-Vergès; Lewis L Lanier; Daniel Weisdorf; Jeffrey S Miller
Journal:  Blood       Date:  2011-12-16       Impact factor: 22.113

Review 2.  Use of NK cell activity in cure by transplant.

Authors:  Wing Leung
Journal:  Br J Haematol       Date:  2011-08-04       Impact factor: 6.998

3.  The association of CMV with NK-cell reconstitution depends on graft source: results from BMT CTN-0201 samples.

Authors:  Armin Rashidi; Xianghua Luo; Sarah Cooley; Claudio Anasetti; Edmund K Waller; Claudio G Brunstein; Frank Cichocki; Daniel J Weisdorf; Jeffrey S Miller
Journal:  Blood Adv       Date:  2019-08-27

4.  CMV reactivation after allogeneic HCT and relapse risk: evidence for early protection in acute myeloid leukemia.

Authors:  Margaret L Green; Wendy M Leisenring; Hu Xie; Roland B Walter; Marco Mielcarek; Brenda M Sandmaier; Stanley R Riddell; Michael Boeckh
Journal:  Blood       Date:  2013-06-06       Impact factor: 22.113

5.  Early human cytomegalovirus replication after transplantation is associated with a decreased relapse risk: evidence for a putative virus-versus-leukemia effect in acute myeloid leukemia patients.

Authors:  Ahmet H Elmaagacli; Nina K Steckel; Michael Koldehoff; Yael Hegerfeldt; Rudolf Trenschel; Markus Ditschkowski; Sandra Christoph; Tanja Gromke; Lambros Kordelas; Hellmut D Ottinger; Rudolf S Ross; Peter A Horn; Susanne Schnittger; Dietrich W Beelen
Journal:  Blood       Date:  2011-05-03       Impact factor: 22.113

6.  Natural killer cell lysis of cytomegalovirus (CMV)-infected cells correlates with virally induced changes in cell surface lymphocyte function-associated antigen-3 (LFA-3) expression and not with the CMV-induced down-regulation of cell surface class I HLA.

Authors:  J M Fletcher; H G Prentice; J E Grundy
Journal:  J Immunol       Date:  1998-09-01       Impact factor: 5.422

7.  Early cytomegalovirus reactivation remains associated with increased transplant-related mortality in the current era: a CIBMTR analysis.

Authors:  Pierre Teira; Minoo Battiwalla; Muthalagu Ramanathan; A John Barrett; Kwang Woo Ahn; Min Chen; Jaime S Green; Ayman Saad; Joseph H Antin; Bipin N Savani; Hillard M Lazarus; Matthew Seftel; Wael Saber; David Marks; Mahmoud Aljurf; Maxim Norkin; John R Wingard; Caroline A Lindemans; Michael Boeckh; Marcie L Riches; Jeffery J Auletta
Journal:  Blood       Date:  2016-02-16       Impact factor: 22.113

8.  γδT cells elicited by CMV reactivation after allo-SCT cross-recognize CMV and leukemia.

Authors:  W Scheper; S van Dorp; S Kersting; F Pietersma; C Lindemans; S Hol; S Heijhuurs; Z Sebestyen; C Gründer; V Marcu-Malina; A Marchant; C Donner; B Plachter; D Vermijlen; D van Baarle; J Kuball
Journal:  Leukemia       Date:  2013-01-01       Impact factor: 11.528

9.  Cytomegalovirus-specific CD8+ T-cells are associated with a reduced incidence of early relapse after allogeneic stem cell transplantation.

Authors:  Pavankumar Reddy Varanasi; Justyna Ogonek; Susanne Luther; Elke Dammann; Michael Stadler; Arnold Ganser; Sylvia Borchers; Lothar Hambach; Eva M Weissinger
Journal:  PLoS One       Date:  2019-03-19       Impact factor: 3.240

10.  CD56dimCD57+NKG2C+ NK cell expansion is associated with reduced leukemia relapse after reduced intensity HCT.

Authors:  F Cichocki; S Cooley; Z Davis; T E DeFor; H Schlums; B Zhang; C G Brunstein; B R Blazar; J Wagner; D J Diamond; M R Verneris; Y T Bryceson; D J Weisdorf; J S Miller
Journal:  Leukemia       Date:  2015-09-29       Impact factor: 11.528

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