Evidence map›Paper›PMID 37168574›Full record

ArticleiScience2023

Intrauterine desensitization enables long term survival of human oligodendrocyte progenitor cells without immunosuppression.

Dou Ye, Suqing Qu, Yinxiang Yang, Zhaoyan Wang, Qian Wang, Weipeng Liu, Fan Zhang, Qian Guan, Xiaohua Wang, Jing Zang and 5 more

Abstract read
In one paragraph

Article in iScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

15 authors.

Dou YeDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Suqing QuDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Yinxiang YangDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Zhaoyan WangDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Qian WangDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Weipeng LiuDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Fan ZhangDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Qian GuanDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Xiaohua WangDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Jing ZangDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Xin LiDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.
Hengtao LiuJiaen Genetics Laboratory, Beijing Jiaen Hospital, Beijing 100191, China.
Ruiqin YaoDepartment of Neurobiology, Xuzhou Key Laboratory of Neurobiology, Xuzhou Medical University, Xuzhou, Jiangsu Province 221004, China.
Zhichun FengFaculty of Pediatrics, The Seventh Medical Centre, Chinese PLA General Hospital, 100700 Beijing, China.
Zuo LuanDepartment of Pediatrics, the Sixth Medical Centre, Chinese PLA General Hospital, Beijing 100037, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune rejection can be reduced using immunosuppressants which are not viable for premature infants. However, desensitization can induce immune tolerance for premature infants because of underdeveloped immune system. The fetuses of Wistar rats at 15-17 days gestation were injected via hOPCs-1 into brain, muscles, and abdomen ex utero and then returned while the fetuses of control without injection. After 6 weeks of desensitization, the brain and muscles were transplanted with hOPCs-1, hNSCs-1, and hOPCs-2. After 10 and 34 weeks of desensitization, hOPCs-1 and hNSCs-1 in desensitized groups was higher than that in the control group while hOPCs-2 were rejected. Treg, CD4CD28, CD8CD28, and CD45RC between the desensitization and the control group differed significantly. Inflammatory cells in group with hOPCs-1 and hNSCs-1 was lower than that in the control group. hOPCs-1 can differentiate into myelin in desensitized groups. Wistar rats with desensitization developed immune tolerance to desensitized and transplanted cells.

Indexed as

ImmunologyNeurologyStem cells research

Identifiers

PMID37168574
PMCPMC10165029

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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.