Killing of Targets by CD8+ T Cells in the Mouse Spleen Follows the Law of Mass Action

被引:33
作者
Ganusov, Vitaly V. [1 ]
Barber, Daniel L. [2 ]
De Boer, Rob J. [3 ]
机构
[1] Univ Tennessee, Dept Microbiol, Knoxville, TN 37996 USA
[2] NIH, Bethesda, MD 20892 USA
[3] Univ Utrecht, Utrecht, Netherlands
关键词
LYMPHOCYTIC CHORIOMENINGITIS VIRUS; MEDIATED CYTO-TOXICITY; IN-VIVO; IMMUNODEFICIENCY-VIRUS; VIRAL-INFECTION; CUTTING EDGE; EFFECTOR FUNCTION; RHESUS-MONKEYS; CTL ACTIVITY; LYMPH-NODES;
D O I
10.1371/journal.pone.0015959
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It has been difficult to correlate the quality of CD8(+) T cell responses with protection against viral infections. To investigate the relationship between efficacy and magnitude of T cell responses, we quantify the rate at which individual CD8(+) effector and memory T cells kill target cells in the mouse spleen. Using mathematical modeling, we analyze recent data on the loss of target cells pulsed with three different peptides from the mouse lymphocytic choriomeningitis virus (LCMV) in mouse spleens with varying numbers of epitope-specific CD8(+) T cells. We find that the killing of targets follows the law of mass-action, i.e., the death rate of individual target cells remains proportional to the frequency (or the total number) of specific CD8(+) T cells in the spleen despite the fact that effector cell densities and effector to target ratios vary about a 1000-fold. The killing rate of LCMV-specific CD8(+) T cells is largely independent of T cell specificity and differentiation stage. Our results thus allow one to calculate the critical T cell concentration at which growth of a virus with a given replication rate can be prevented from the start of infection by memory CD8(+) T cell response.
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页数:8
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