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CXCR3 and IFN Protein-10 in Pneumocystis Pneumonia

Florencia McAllister^1,*, Sanbao Ruan^1,, Chad Steele^*, Mingquan Zheng^*, Laura McKinley^*, Lauren Ulrich^*, Luis Marrero, Judd E. Shellito and Jay K. Kolls^2,*

^* Children’s Hospital of Pittsburgh, University of Pittsburgh, Department of Pediatrics, Pittsburgh, PA 15213; and Louisiana State University Health Sciences Center Gene Therapy Program, Louisiana State University Health Sciences Center School of Medicine, New Orleans, LA 70112

We have previously shown that Tc1 CD8⁺ T cells have in vitro and in vivo effector activity against Pneumocystis (PC) infection in mice. Because these cells have preferential expression of CXCR3, we investigated whether CXCR3 was required for host defense activity against PC. Mice deficient in CXCR3 but CD4⁺ T cell intact, showed an initial delay but were able to clear the infectious challenge, indicating that CXCR3 signaling is not essential for clearance of PC. CD4-depleted mice had lower levels of monokine induced by IFN-, IFN protein-10 (IP-10), and IFN-inducible T cell -chemoattractant at day 7 of infection and are permissive to PC infection. Overexpression of IP-10 in the lungs by adenoviral gene transfer did not accelerate clearance of infection in control mice but accelerated clearance by day 28 in mice depleted of CD4⁺ T cells. This effect was associated with increased recruitment of CD8⁺ T to the lungs with higher CXCR3⁺ expression levels and enhanced IFN- secretion upon in vitro activation compared with control mice. These results indicate that the CXCR3 chemokines are part of the host defense response to PC, and that IP-10 can direct Tc1 CD8⁺ T cell recruitment to the lungs and contribute to host defense against PC even in the absence of CD4⁺ T cells.

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