Evidence map›Paper›PMID 32381589›Full record

ArticleScience (New York, N.Y.)2020

PIRs mediate innate myeloid cell memory to nonself MHC molecules.

Hehua Dai, Peixiang Lan, Daqiang Zhao, Khodor Abou-Daya, Wentao Liu, Wenhao Chen, Andrew J Friday, Amanda L Williams, Tao Sun, Jianjiao Chen and 16 more

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

77 citing papers in PubMed, 149 citations in OpenAlex.

  1. Innate Immune Memory Responses in Organ Transplantation.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
  2. Trained Memory of Uterine Macrophages Improves Subsequent Pregnancy Outcomes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. The authors respond to feedback onFrontiers in oncology · 2026
    Article
  8. Sensitization in Transplantation Assessment of Risk 2025 innate working group: The potential role of innate allorecognition in kidney allograft damage.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Review
  9. Review
  10. Donor-recipient mismatch at theScience translational medicine · 2025
    Article
  11. Article
  12. Setdb1 ablation in macrophages attenuates fibrosis in heart allografts.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Review
  14. Adenosine triphosphate-mediated signaling of P2X7 receptors controls donor extracellular vesicle release and major histocompatibility complex cross-decoration after allotransplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 7 institutions in 4 countries.

Hehua Dai *Thomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-1595-5737
Peixiang Lan *Immunobiology and Transplant Science Center, Houston Methodist Research Institute, Houston, TX, USA.ORCID 0000-0001-7569-894X
Daqiang Zhao *Thomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0003-2582-0112
Khodor Abou-DayaThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0001-8788-2728
Wentao LiuImmunobiology and Transplant Science Center, Houston Methodist Research Institute, Houston, TX, USA.
Wenhao ChenImmunobiology and Transplant Science Center, Houston Methodist Research Institute, Houston, TX, USA.
Andrew J FridayThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Amanda L WilliamsThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Tao SunDepartment of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Jianjiao ChenDepartment of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Wei ChenDepartment of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0001-7196-8703
Steven Mortin-TothProgram in Genetics and Genome Biology, Hospital for Sick Children Research Institute, Toronto, ON, Canada.ORCID 0000-0002-3029-1975
Jayne S DanskaProgram in Genetics and Genome Biology, Hospital for Sick Children Research Institute, Toronto, ON, Canada.ORCID 0000-0002-6549-4991
Chris WiebeDepartment of Medicine, University of Manitoba, Winnipeg, MB, Canada.
Peter NickersonDepartment of Medicine, University of Manitoba, Winnipeg, MB, Canada.
Tengfang LiThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0001-6345-6716
Lisa R MathewsThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Hêth R TurnquistThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-4173-4014
Matthew L NicotraThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0001-5361-8398
Sebastien GingrasDepartment of Immunology, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0003-2607-8642
Eiji TakayamaDepartment of Oral Biochemistry, Asahi University School of Dentistry, Gifu, Japan.
Hiromi KubagawaHumoral Immune Regulation, Deutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany.
Mark J ShlomchikDepartment of Immunology, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-2152-0959
Martin H OberbarnscheidtThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA. mho6@pitt.edu xcli@houstonmethodist.org lakkisf@upmc.edu.ORCID 0000-0003-2040-809X
Xian C LiImmunobiology and Transplant Science Center, Houston Methodist Research Institute, Houston, TX, USA. mho6@pitt.edu xcli@houstonmethodist.org lakkisf@upmc.edu.ORCID 0000-0002-5981-2762
Fadi G LakkisThomas E. Starzl Transplantation Institute and Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA. mho6@pitt.edu xcli@houstonmethodist.org lakkisf@upmc.edu.ORCID 0000-0001-9937-2637
University of Pittsburgh · USHouston Methodist · USUniversity of Manitoba · CAAsahi University · JPGerman Rheumatism Research Centre · DEHospital for Sick Children · CAUniversity of Toronto · CA

Funding

Modulation of innate immune cells to create transplant toleranceR01AI080779 · NIAID · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Xian Chang Li · 2011 to 2026
$5.2M
Immunoregulatory Mechanisms of IL-33 in Heart TransplantationR01HL122489 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Heth R Turnquist · 2015 to 2026
$4.9M
Innate Recognition of Allogeneic Non-SelfR01AI099465 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAKKIS, FADI G. · 2012 to 2022
$4.1M
Tertiary Lymphoid Organs in TransplantationR01AI145881 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI OBERBARNSCHEIDT, MARTIN H · 2019 to 2023
$1.9M
Modulation of innate immune cells to create transplant toleranceR56AI080779 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI LI, XIAN CHANG · 2010 to 2010
$435k
CIHRNHLBI NIH HHS R01 HL122489NIAID NIH HHS R01 AI080779NIAID NIH HHS R01 AI099465NIAID NIH HHS R01 AI145881NIAID NIH HHS R56 AI080779
6 · The paper itself

Abstract

Immunological memory specific to previously encountered antigens is a cardinal feature of adaptive lymphoid cells. However, it is unknown whether innate myeloid cells retain memory of prior antigenic stimulation and respond to it more vigorously on subsequent encounters. In this work, we show that murine monocytes and macrophages acquire memory specific to major histocompatibility complex I (MHC-I) antigens, and we identify A-type paired immunoglobulin-like receptors (PIR-As) as the MHC-I receptors necessary for the memory response. We demonstrate that deleting PIR-A in the recipient or blocking PIR-A binding to donor MHC-I molecules blocks memory and attenuates kidney and heart allograft rejection. Thus, innate myeloid cells acquire alloantigen-specific memory that can be targeted to improve transplant outcomes.

Indexed as

Immunity, InnateImmunologic MemoryAnimalsGene DeletionGraft RejectionHeart TransplantationHistocompatibility Antigens Class IKidney TransplantationMacrophagesMiceMice, Inbred BALB CMice, Mutant StrainsMonocytesReceptors, ImmunologicHistocompatibility Antigens Class IPira1 protein, mousePira3 protein, mouseReceptors, ImmunologicSirpa protein, mouse

Identifiers

PMID32381589
PMCPMC7379379
OpenAlexW3023788516

What OpenQuestion holds

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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.