Immune Response Resetting in Ongoing Sepsis

• Published in: The Journal of immunology (1950) Vol. 203; no. 5; pp. 1298 - 1312
• Main Authors: Nowill, Alexandre E, Fornazin, Márcia C, Spago, Maria C, Dorgan Neto, Vicente, Pinheiro, Vitória R P, Alexandre, Simônia S S, Moraes, Edgar O, Souza, Gustavo H M F, Eberlin, Marcos N, Marques, Lygia A, Meurer, Eduardo C, Franchi, Jr, Gilberto C, de Campos-Lima, Pedro O
• Format: Journal Article
• Language: English
• Published: United States AAI 01.09.2019
• Subjects: Animals; Apoptosis - immunology; CD3 Complex - immunology; CD8-Positive T-Lymphocytes - immunology; Cecum - immunology; Cytokines - immunology; Disease Models, Animal; Female; Immunologic Memory - immunology; Infectious Disease and Host Response; Inflammation - immunology; Lipidomics - methods; Lysophosphatidylcholines - immunology; Mice; Mice, Inbred C57BL; Phosphatidylcholines - immunology; Proteomics - methods; Sepsis - immunology; Shock, Septic - immunology; Spleen - immunology
• ISSN: 0022-1767; 1550-6606; 1550-6606
• DOI: 10.4049/jimmunol.1900104

Cure of severe infections, sepsis, and septic shock with antimicrobial drugs is a challenge because morbidity and mortality in these conditions are essentially caused by improper immune response. We have tested the hypothesis that repeated reactivation of established memory to pathogens may reset unfavorable immune responses. We have chosen for this purpose a highly stringent mouse model of polymicrobial sepsis by cecum ligation and puncture. Five weeks after priming with a diverse Ag pool, high-grade sepsis was induced in C57BL/6j mice that was lethal in 24 h if left untreated. Antimicrobial drug (imipenem) alone rescued 9.7% of the animals from death, but >5-fold higher cure rate could be achieved by combining imipenem and two rechallenges with the Ag pool ( < 0.0001). Antigenic stimulation fine-tuned the immune response in sepsis by contracting the total CD3 T cell compartment in the spleen and disengaging the hyperactivation state in the memory T subsets, most notably CD8 T cells, while preserving the recovery of naive subsets. Quantitative proteomics/lipidomics analyses revealed that the combined treatment reverted the molecular signature of sepsis for cytokine storm, and deregulated inflammatory reaction and proapoptotic environment, as well as the lysophosphatidylcholine/phosphatidylcholine ratio. Our results showed the feasibility of resetting uncontrolled hyperinflammatory reactions into ordered hypoinflammatory responses by memory reactivation, thereby reducing morbidity and mortality in antibiotic-treated sepsis. This beneficial effect was not dependent on the generation of a pathogen-driven immune response itself but rather on the reactivation of memory to a diverse Ag pool that modulates the ongoing response.