Evidence map›Paper›PMID 25676063›Full record

ArticleExperimental & molecular medicine2015

Subdominant H60 antigen-specific CD8 T-cell response precedes dominant H4 antigen-specific response during the initial phase of allogenic skin graft rejection.

Kang Il Yoo, Ji Yeong Jeon, Su Jeong Ryu, Giri Nam, Hyewon Youn, Eun Young Choi

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Kang Il YooDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
Ji Yeong JeonDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
Su Jeong RyuDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
Giri NamDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
Hyewon Youn1] Department of Nuclear Medicine, Cancer Imaging Center, Seoul National University Hospital, Seoul, Korea [2] Tumor Microenvironment Global Core Research Center, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Eun Young ChoiDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea.
Seoul National University · KRSeoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In allogeneic transplantation, including the B6 anti-BALB.B settings, H60 and H4 are two representative dominant minor histocompatibility antigens that induce strong CD8 T-cell responses. With different distribution patterns, H60 expression is restricted to hematopoietic cells, whereas H4 is ubiquitously expressed. H60-specific CD8 T-cell response has been known to be dominant in most cases of B6 anti-BALB.B allo-responses, except in the case of skin transplantation. To understand the mechanism underlying the subdominance of H60 during allogeneic skin transplantation, we investigated the dynamics of the H60-specific CD8 T cells in B6 mice transplanted with allogeneic BALB.B tail skin. Unexpectedly, longitudinal bioluminescence imaging and flow cytometric analyses revealed that H60-specific CD8 T cells were not always subdominant to H4-specific cells but instead showed a brief dominance before the H4 response became predominant. H60-specific CD8 T cells could expand in the draining lymph node and migrate to the BALB.B allografts, indicating their active participation in the anti-BALB.B allo-response. Enhancing the frequencies of H60-reactive CD8 T cells prior to skin transplantation reversed the immune hierarchy between H60 and H4. Additionally, H60 became predominant when antigen presentation was limited to the direct pathway. However, when antigen presentation was restricted to the indirect pathway, the expansion of H60-specific CD8 T cells was limited, whereas H4-specific CD8 T cells expanded significantly, suggesting that the temporary immunodominance and eventual subdominance of H60 could be due to their reliance on the direct antigen presentation pathway. These results enhance our understanding of the immunodominance phenomenon following allogeneic tissue transplantation.

Indexed as

Skin TransplantationAnimalsAntigen PresentationAntigen-Presenting CellsCD8-Positive T-LymphocytesEpitopes, T-LymphocyteFemaleGraft RejectionInterferon-gammaLymphocyte ActivationLymphocyte CountMiceMinor Histocompatibility AntigensTransplantation, HomologousEpitopes, T-LymphocyteInterferon-gammaminor H antigen H60Minor Histocompatibility Antigens

Identifiers

PMID25676063
PMCPMC4346485
OpenAlexW2143548188

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.