دورية أكاديمية

GATA2 haploinsufficient patients lack innate lymphoid cells that arise after hematopoietic cell transplantation

التفاصيل البيبلوغرافية
العنوان: GATA2 haploinsufficient patients lack innate lymphoid cells that arise after hematopoietic cell transplantation
المؤلفون: Y. F. van Lier, L. Krabbendam, N. J. E. Haverkate, S. S. Zeerleder, C. E. Rutten, B. Blom, H. Spits, M. D. Hazenberg
المصدر: Frontiers in Immunology, Vol 13 (2022)
بيانات النشر: Frontiers Media S.A., 2022.
سنة النشر: 2022
المجموعة: LCC:Immunologic diseases. Allergy
مصطلحات موضوعية: innate lymphocyte cells (ILCs), NK cells, GATA 2, allogeneic haematopoietic cell transplantation, reconstitution, MonoMAC syndrome, Immunologic diseases. Allergy, RC581-607
الوصف: Innate lymphoid cells (ILC) are important barrier tissue immune regulators. They play a pivotal role in early non-specific protection against infiltrating pathogens, regulation of epithelial integrity, suppression of pro-inflammatory immune responses and shaping the intestinal microbiota. GATA2 haploinsufficiency causes an immune disorder that is characterized by bone marrow failure and (near) absence of monocytes, dendritic cells, B cells and natural killer (NK) cells. T cells develop normally, albeit at lower numbers. Here, we describe the absence of ILCs and their progenitors in blood and bone marrow of two patients with GATA2 haploinsufficiency and show that all subsets of ILCs appear after allogeneic hematopoietic stem cell transplantation, irrespective of the preparative conditioning regimen. Our data indicate that GATA2 is involved in the development of hematopoietic precursor cells (HPC) towards the ILC lineage.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1664-3224
العلاقة: https://www.frontiersin.org/articles/10.3389/fimmu.2022.1020590/fullTest; https://doaj.org/toc/1664-3224Test
DOI: 10.3389/fimmu.2022.1020590
الوصول الحر: https://doaj.org/article/eb574ab2ffc84f22a578dca8b8f8a74bTest
رقم الانضمام: edsdoj.b574ab2ffc84f22a578dca8b8f8a74b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16643224
DOI:10.3389/fimmu.2022.1020590