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May 1, 1977Proceedings of the National Academy of Sciences239 citationsOpen Access

Enhancement of nonspecific immunity to Klebsiella pneumoniae infection by a synthetic immunoadjuvant (N-acetylmuramyl-L-alanyl-D-isoglutamine) and several analogs.

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LCL ChedidInstitut PasteurMPM ParantCentre National de la Recherche ScientifiqueFPFrançois ParantHospices Civils de Lyon

Key Points

  • The aim is to evaluate the effect of synthetic immunoadjuvants on enhancing nonspecific immunity against Klebsiella pneumoniae infection in mice.
  • Tested N-acetylmuramyl-L-alanyl-D-isoglutamine and four analogs in a mouse model of infection.
  • Administered adjuvants via various routes, including oral, and post-infection challenge.
  • Compared their effectiveness against seventeen other analog adjuvants and assessed immunogenicity.
  • N-acetylmuramyl-L-alanyl-D-isoglutamine significantly enhances nonspecific immunity to Klebsiella pneumoniae compared to control.
  • None of the seventeen other analogs significantly improved resistance to infection; seven were active only in saline.
  • Synthetic adjuvants showed no toxicity, immunogenicity, or mitogenicity in normal or adrenalectomized mice.

Abstract

N-Acetylmuramyl-L-alanyl-D-isoglutamine and four other synthetic adjuvants that are structural analogs of part of the mycobacterial peptidoglycan monomer are shown to enhance the nonspecific immunity of mice infected by Klebsiella pneumoniae. These compounds are active by various routes, including oral administration; they are also effective when administered after challenge. Of the seventeen other analogs tested, none is able to increase significantly resistance to infection, although seven of these molecules are adjuvant-active in saline. Previous results have shown that in contrast to lipopolysaccharides, these synthetic adjuvants are devoid of immunogenicity, mitogenicity, and toxicity in normal or adrenalectomized mice.

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Cite This Study

Chedid et al. (1977) studied this question.

synapsesocial.com/papers/6a0cf93faf467f299a7c7b4bhttps://doi.org/10.1073/pnas.74.5.2089
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