Bead-isolated human CD4+CD25+ T regulatory cells are anergic and significantly suppress proliferation of CD4+CD25- T responder cells

Eyad Elkord; Lucy Hopcraft; Debbie Burt; Peter L. Stern

doi:10.1016/j.clim.2006.02.007

Bead-isolated human CD4⁺CD25⁺ T regulatory cells are anergic and significantly suppress proliferation of CD4⁺CD25^- T responder cells

Eyad Elkord^*, Lucy Hopcraft, Debbie Burt, Peter L. Stern

^*Corresponding author for this work

Research output: Contribution to journal › Letter › peer-review

5 Citations (Scopus)

Original language	English
Pages (from-to)	232-233
Number of pages	2
Journal	Clinical Immunology
Volume	120
Issue number	2
DOIs	https://doi.org/10.1016/j.clim.2006.02.007
Publication status	Published - Aug 2006
Externally published	Yes

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10.1016/j.clim.2006.02.007

Cite this

@article{f39c42c983404a349e864368f050f382,

title = "Bead-isolated human CD4+CD25+ T regulatory cells are anergic and significantly suppress proliferation of CD4+CD25- T responder cells",

author = "Eyad Elkord and Lucy Hopcraft and Debbie Burt and Stern, \{Peter L.\}",

year = "2006",

month = aug,

doi = "10.1016/j.clim.2006.02.007",

language = "English",

volume = "120",

pages = "232--233",

journal = "Clinical Immunology",

issn = "1521-6616",

number = "2",

}

TY - JOUR

T1 - Bead-isolated human CD4+CD25+ T regulatory cells are anergic and significantly suppress proliferation of CD4+CD25- T responder cells

AU - Elkord, Eyad

AU - Hopcraft, Lucy

AU - Burt, Debbie

AU - Stern, Peter L.

PY - 2006/8

Y1 - 2006/8

UR - https://www.scopus.com/pages/publications/33746036816

U2 - 10.1016/j.clim.2006.02.007

DO - 10.1016/j.clim.2006.02.007

M3 - Letter

C2 - 16581298

AN - SCOPUS:33746036816

SN - 1521-6616

VL - 120

SP - 232

EP - 233

JO - Clinical Immunology

JF - Clinical Immunology

IS - 2

ER -

Bead-isolated human CD4+CD25+ T regulatory cells are anergic and significantly suppress proliferation of CD4+CD25- T responder cells

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Bead-isolated human CD4⁺CD25⁺ T regulatory cells are anergic and significantly suppress proliferation of CD4⁺CD25^- T responder cells