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Items: 1 to 20 of 218

1.

Lymphocyte activation gene-3 (CD223) regulates the size of the expanding T cell population following antigen activation in vivo.

Workman CJ, Cauley LS, Kim IJ, Blackman MA, Woodland DL, Vignali DA.

J Immunol. 2004 May 1;172(9):5450-5.

2.
3.

Negative regulation of T cell homeostasis by lymphocyte activation gene-3 (CD223).

Workman CJ, Vignali DA.

J Immunol. 2005 Jan 15;174(2):688-95.

4.
6.

Apparent MHC-independent stimulation of CD8+ T cells in vivo during latent murine gammaherpesvirus infection.

Coppola MA, Flaño E, Nguyen P, Hardy CL, Cardin RD, Shastri N, Woodland DL, Blackman MA.

J Immunol. 1999 Aug 1;163(3):1481-9.

7.

T cell- and perforin-dependent depletion of B cells in vivo by staphylococcal enterotoxin A.

Sundstedt A, Grundström S, Dohlsten M.

Immunology. 1998 Sep;95(1):76-82.

8.

During viral infection of the respiratory tract, CD27, 4-1BB, and OX40 collectively determine formation of CD8+ memory T cells and their capacity for secondary expansion.

Hendriks J, Xiao Y, Rossen JW, van der Sluijs KF, Sugamura K, Ishii N, Borst J.

J Immunol. 2005 Aug 1;175(3):1665-76.

9.

The OX40 costimulatory receptor determines the development of CD4 memory by regulating primary clonal expansion.

Gramaglia I, Jember A, Pippig SD, Weinberg AD, Killeen N, Croft M.

J Immunol. 2000 Sep 15;165(6):3043-50.

10.
11.

Antigen-specific CD8+ T cell clonal expansions develop from memory T cell pools established by acute respiratory virus infections.

Ely KH, Ahmed M, Kohlmeier JE, Roberts AD, Wittmer ST, Blackman MA, Woodland DL.

J Immunol. 2007 Sep 15;179(6):3535-42.

12.

Bacterial superantigens reactivate antigen-specific CD8+ memory T cells.

Coppola MA, Blackman MA.

Int Immunol. 1997 Sep;9(9):1393-403.

PMID:
9310843
13.

Differential requirements for survival and proliferation of CD8 naïve or memory T cells.

Tanchot C, Lemonnier FA, Pérarnau B, Freitas AA, Rocha B.

Science. 1997 Jun 27;276(5321):2057-62.

14.

Continuous exposure of mice to superantigenic toxins induces a high-level protracted expansion and an immunological memory in the toxin-reactive CD4+ T cells.

Chen L, Koyanagi M, Fukada K, Imanishi K, Yagi J, Kato H, Miyoshi-Akiyama T, Zhang R, Miwa K, Uchiyama T.

J Immunol. 2002 Apr 15;168(8):3817-24.

15.

IL-2 secretion by CD4+ T cells in vivo is rapid, transient, and influenced by TCR-specific competition.

Sojka DK, Bruniquel D, Schwartz RH, Singh NJ.

J Immunol. 2004 May 15;172(10):6136-43.

16.

Regulation of follicular dendritic cell networks by activated T cells: the role of CD137 signaling.

Sun Y, Blink SE, Chen JH, Fu YX.

J Immunol. 2005 Jul 15;175(2):884-90.

17.

Distribution of cycling T lymphocytes in blood and lymphoid organs during immune responses.

Vasseur F, Le Campion A, Pavlovitch JH, Pénit C.

J Immunol. 1999 May 1;162(9):5164-72.

18.

B7-2 (CD86) controls the priming of autoreactive CD4 T cell response against pancreatic islets.

Yadav D, Judkowski V, Flodstrom-Tullberg M, Sterling L, Redmond WL, Sherman L, Sarvetnick N.

J Immunol. 2004 Sep 15;173(6):3631-9.

19.
20.

Activated antigen-specific CD8+ T cells persist in the lungs following recovery from respiratory virus infections.

Hogan RJ, Usherwood EJ, Zhong W, Roberts AA, Dutton RW, Harmsen AG, Woodland DL.

J Immunol. 2001 Feb 1;166(3):1813-22.

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