Evidence map›Paper›PMID 21917752›Full record

ArticleBlood2011

Memory T cells from minor histocompatibility antigen-vaccinated and virus-immune donors improve GVL and immune reconstitution.

Ning Li, Catherine Matte-Martone, Hong Zheng, Weiguo Cui, Srividhya Venkatesan, Hung Sheng Tan, Jennifer McNiff, Anthony J Demetris, Derry Roopenian, Susan Kaech and 1 more

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 50 citations in OpenAlex.

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  15. Prevention and Treatment of Acute Graft-versus-Host Disease in Children, Adolescents, and Young Adults.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Ning LiDepartment of Medicine, Yale University School of Medicine Cancer Center, New Haven, CT 06520-8032, USA.
Catherine Matte-Martone
Hong Zheng
Weiguo Cui
Srividhya Venkatesan
Hung Sheng Tan
Jennifer McNiff
Anthony J Demetris
Derry Roopenian
Susan Kaech
Warren D Shlomchik
Jackson Laboratory · USUniversity of Pittsburgh · USYale Cancer Center · US

Funding

Leukemia Stem Cells: Essential Targets for GVL and Mediators of GVL-ResistanceR01CA096943 · NCI · YALE UNIVERSITY · PI SHLOMCHIK, WARREN D · 2003 to 2013
$2.8M
Transfusion of Donor Effector Memory T Cells for GVL and Immune ReconstitutionR01HL109599 · NHLBI · YALE UNIVERSITY · PI SHLOMCHIK, MARK J, SHLOMCHIK, WARREN D · 2011 to 2015
$2.0M
NCI NIH HHS CA096943NCI NIH HHS R01 CA096943NHLBI NIH HHS R01 HL109599
6 · The paper itself

Abstract

Donor T cells contribute to the success of allogeneic hematopoietic stem cell transplantation (alloSCT). Alloreactive donor T cells attack leukemia cells, mediating the GVL effect. Donor T cells, including the memory T cells (T(M)) that are generated after infection, also promote immune reconstitution. Nonetheless, leukemia relapse and infection are major sources of treatment failure. Efforts to augment GVL and immune reconstitution have been limited by GVHD, the attack by donor T cells on host tissues. One approach to augmenting GVL has been to infuse ex vivo-generated T cells with defined specificities; however, this requires expertise that is not widely available. In the present study, we tested an alternative approach, adoptive immunotherapy with CD8+ T(M) from donors vaccinated against a single minor histocompatibility antigen (miHA) expressed by leukemia cells. Vaccination against the miHA H60 greatly augmented T(M)-mediated GVL against mouse chronic-phase (CP-CML) and blast crisis chronic myeloid leukemia (BC-CML). T(M)-mediated GVL was antigen specific and was optimal when H60 expression was hematopoietically restricted. Even when H60 was ubiquitous, donor H60 vaccination had a minimal impact on GVHD. T(M) from lymphocytic choriomeningitis virus (LCMV)-immune and H60-vaccinated donors augmented GVL and protected recipients from LCMV. These data establish a strategy for augmenting GVL and immune reconstitution without elaborate T-cell manipulation.

Indexed as

Immunologic MemoryTissue DonorsVaccinationAnimalsCell ProliferationGraft vs Leukemia EffectHematopoiesisLymphocytesLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMiceMice, Inbred C3HMice, Inbred C57BLMice, KnockoutMinor Histocompatibility AntigensT-Lymphocytesminor H antigen H60Minor Histocompatibility Antigens

Identifiers

PMID21917752
PMCPMC3228506
OpenAlexW1994712778

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.