Macrophage-derived insulin-like growth factor-1 affects influenza vaccine efficacy through the regulation of immune cell homeostasis. Issue 36 (24th August 2017)

• Record Type: Journal Article
• Authors: Yoon, Il-Sub; Park, Hyelim; Kwak, Hye-Won; Woo Jung, Yong; Nam, Jae-Hwan
• Is Part Of: Vaccine. Volume 35:Issue 36(2017)
• Page Start: 4687
• Page End: 4694
• Publication Date: 2017-08-24
• Subjects: Influenza vaccine -- Insulin-like growth factor-1 -- Macrophages -- Th1 -- Th17; Vaccines -- Periodicals; 615.372
• DOI: 10.1016/j.vaccine.2017.07.037
• Languages: English
• ISSNs: 0264-410X

Abstract

Highlights: A variety of host factors affects vaccine-induced antibody level. Insulin-like growth factor-1 (IGF-1) plays an important role in immune response. Macrophage-derived IGF-1 affects the vaccine-triggered immune response. IGF-1 regulates the immune cell homeostasis. Abstract: The level of antibody production induced by a vaccine involves a variety of host factors. One of these, insulin-like growth factor-1 (IGF-1), plays an important role in lymphocyte maturation and antibody expression. Here, we investigated the role of macrophage-derived IGF-1 in the induction of influenza vaccine-specific antibodies using macrophage-derived IGF-1 gene knockout (MIKO) mice. The titers of vaccine-specific total immunoglobulin G (IgG) and IgG1 after immunization were about two- to fourfold lower in MIKO mice than in WT mice. Moreover, MIKO mice showed a relatively weak booster effect of repeated immunization. In contrast, antigen-nonspecific total IgG was about threefold higher in MIKO mice than in WT mice. After viral challenge, the viral titer and the pathological damage in lungs of MIKO mice were higher than those in WT mice despite vaccination. Interestingly, the proportions of proinflammatory immune cells including M1 macrophages, Th1 and Th17 cells was higher in unvaccinated MIKO mice than in unvaccinated WT mice. This suggests that nonspecific activation of immune cells may paradoxically impair the response to the vaccine. In addition, although the proportions of T follicular helper (Tfh) cells and GL-7 + germinal center (GC) B cells were higher in MIKO mice than in WT mice, the population of CD138 + B220 + antibody-secreting plasmablasts was lower in MIKO mice, which may be a cause of the low influenza-specific antibody titer in MIKO mice. Taken together, these results suggest that macrophage-derived IGF-1 might play an important role in the vaccine-triggered immune response by regulating immune cell homeostasis.