Pathogen-specific memory T cells (T) contribute to enhanced immune protection under conditions of reinfection, and their effective recruitment into a recall response relies, in part, on cues imparted by chemokines that coordinate their spatiotemporal positioning. An integrated perspective, however, needs to consider T as a potentially relevant chemokine source themselves. In this study, we employed a comprehensive transcriptional/translational profiling strategy to delineate the identities, expression patterns, and dynamic regulation of chemokines produced by murine pathogen-specific T CD8T, and to a lesser extent CD4T, are a prodigious source for six select chemokines (CCL1/3/4/5, CCL9/10, and XCL1) that colle... More
Pathogen-specific memory T cells (T) contribute to enhanced immune protection under conditions of reinfection, and their effective recruitment into a recall response relies, in part, on cues imparted by chemokines that coordinate their spatiotemporal positioning. An integrated perspective, however, needs to consider T as a potentially relevant chemokine source themselves. In this study, we employed a comprehensive transcriptional/translational profiling strategy to delineate the identities, expression patterns, and dynamic regulation of chemokines produced by murine pathogen-specific T CD8T, and to a lesser extent CD4T, are a prodigious source for six select chemokines (CCL1/3/4/5, CCL9/10, and XCL1) that collectively constitute a prominent and largely invariant signature across acute and chronic infections. Notably, constitutive CCL5 expression by CD8T serves as a unique functional imprint of prior antigenic experience; induced CCL1 production identifies highly polyfunctional CD8 and CD4T subsets; long-term CD8T maintenance is associated with a pronounced increase of XCL1 production capacity; chemokines dominate the earliest stages of the CD8T recall response because of expeditious synthesis/secretion kinetics (CCL3/4/5) and low activation thresholds (CCL1/3/4/5/XCL1); and T chemokine profiles modulated by persisting viral Ags exhibit both discrete functional deficits and a notable surplus. Nevertheless, recall responses and partial virus control in chronic infection appear little affected by the absence of major T chemokines. Although specific contributions of T-derived chemokines to enhanced immune protection therefore remain to be elucidated in other experimental scenarios, the ready visualization of T chemokine-expression patterns permits a detailed stratification of T functionalities that may be correlated with differentiation status, protective capacities, and potential fates.
