Differences in <scp>H3K4me3</scp> and chromatin accessibility contribute to altered T‐cell receptor signaling in neonatal naïve <scp>CD4</scp> T cells-Reference-Cited by-同舟云学术

Differences in H3K4me3 and chromatin accessibility contribute to altered T‐cell receptor signaling in neonatal naïve CD4 T cells

Published:2022-06-20 Issue:7 Volume:100 Page:562-579
ISSN:0818-9641
Container-title:Immunology & Cell Biology
language:en
Short-container-title:Immunol Cell Biol

Author:

Bermick Jennifer R¹²^ORCID,Issuree Priya³,denDekker Aaron⁴,Gallagher Katherine A⁴,Santillan Donna⁵,Kunkel Steven⁶,Lukacs Nicholas⁶⁷,Schaller Matthew⁶⁸

Affiliation:

1. Division of Neonatology, Department of Pediatrics University of Iowa Iowa City IA USA

2. Division of Neonatal‐Perinatal Medicine, Department of Pediatrics Michigan Medicine Ann Arbor MI USA

3. Department of Internal Medicine University of Iowa Iowa City IA USA

4. Department of Vascular Surgery Michigan Medicine Ann Arbor MI USA

5. Department of Obstetrics and Gynecology University of Iowa Iowa City IA USA

6. Department of Pathology Michigan Medicine Ann Arbor MI USA

7. Mary H. Weiser Food Allergy Center Michigan Medicine Ann Arbor MI USA

8. Pulmonary, Critical Care & Sleep Medicine University of Florida Gainesville FL USA

Funder

University of Michigan

Publisher

Wiley

Subject

Cell Biology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/imcb.12561

Reference47 articles.

1. Global, regional, and national causes of under-5 mortality in 2000–15: an updated systematic analysis with implications for the Sustainable Development Goals

2. Zymosan Induces Immune Responses Comparable with Those of Adults in Monocytes, Dendritic Cells, and Monocyte-Derived Dendritic Cells from Cord Blood

3. Cytokine Expression in Response to Bacterial Antigens in Preterm and Term Infant Cord Blood Monocytes

4. Cord blood CD4 CD45RA T cells achieve a lower magnitude of activation when compared with their adult counterparts

5. Distinctive response of naïve lymphocytes from cord blood to primary activation via TCR

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