Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Recall and propagation of allospecific memory T cells independent of secondary lymphoid organs.

Proceedings of the National Academy of Sciences of the United States of America - 30 Apr 2002

Chalasani Geetha, Dai Zhenhua, Konieczny Bogumila T, Baddoura Fady K, Lakkis Fadi G

Abstract excerpt

The allospecifc T cell population responding to a transplanted organ consists of both naive and memory lymphocytes. Although it is established that naive T cells are activated by antigen within the organized structures of secondary lymphoid organs (the spleen, lymph nodes, and mucosal lymphoid tissues), it is not clear whether memory T cell activation and propagation depend on homing to these organs. To answer...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cell Transplantation
Share to Immunologic Memory

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Immunophenotyping

Share to Lymph Nodes

Share to Mucous Membrane

Share to Spleen

Share to T-Lymphocyte Subsets

Share to T-Lymphocytes, Cytotoxic

Source

Open in PubMed Open full text

Identifiers

PMID: 11983909
DOI: 10.1073/pnas.092596999
PMCID: PMC122922

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Recall and propagation of allospecific memory T cells independent of secondary lymphoid organs.PMID 11983909Read ↗

Memory T Cells in Transplantation: Old Challenges Define New Directions.Semantic proximity Read ↗

Tracing Donor-MHC Class II Reactive B cells in Mouse Cardiac Transplantation: Delayed CTLA4-Ig Treatment Prevents Memory Alloreactive B-Cell Generation.Semantic proximity Read ↗

Memory T cells in allograft rejection.Semantic proximity Read ↗

Homeostatic Proliferation of Lymphocytes Results in Augmented Memory-Like Function and Accelerated Allograft RejectionSemantic proximity Read ↗

A repertoire-independent and cell-intrinsic defect in murine GVHD induction by effector memory T cells.Semantic proximity Read ↗

High-resolution characterization of cytokine-producing alloreactivity in naive and allograft-primed mice.Semantic proximity Read ↗

Alloreactive Memory T Cells Are Responsible for the Persistence of Graft-versus-Host DiseaseSemantic proximity Read ↗

Inability of memory T cells to induce graft-versus-host disease is a result of an abortive alloresponseSemantic proximity Read ↗

Alloreactive T cells that do not require TCR and CD8 coengagement are present in naive mice and contribute to graft rejection.Semantic proximity Read ↗

Persisting alloantigen prevents primed CD45RC- CD4 T cells from inducing allograft rejection: implications for immunological memory.Semantic proximity Read ↗

PD-L1 Prevents the Development of Autoimmune Heart Disease in Graft-versus-Host DiseaseSemantic proximity Read ↗

Donor CD4+ T and B cells in transplants induce chronic graft-versus-host disease with autoimmune manifestationsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.