AI Article Synopsis

  • Vaccines can trigger broader immune responses beyond their intended targets, known as heterologous effects.
  • In a study, two monoclonal antibodies (mAbs) specific to tetanus (mAb26 and mAb51) were tested for their ability to protect against chlamydial infection.
  • Results showed that mAb26 significantly outperformed mAb51 in preventing infection in lab tests and reducing disease severity in guinea pigs, suggesting that tetanus immunization can create protective antibodies against other infections like Chlamydia.

Article Abstract

Vaccines can have heterologous effects on the immune system, i.e., effects other than triggering an immune response against the disease targeted by the vaccine. We investigated whether monoclonal antibodies (mAbs) specific for tetanus could cross-react with Chlamydia and confer heterologous protection against chlamydial infection. The capability of two tetanus-specific mAbs, namely mAb26 and mAb51, to prevent chlamydial infection has been assessed: (i) in vitro, by performing a neutralization assay using human conjunctival epithelial (HCjE) cells infected with serovar B, and (ii) in vivo, by using a guinea pig model of -induced inclusion conjunctivitis. The mAb26 has been superior in comparison with mAb51 in the prevention of chlamydial infection in HCjE cells. The mAb26 has conferred ≈40% inhibition of the infection, compared to less than 5% inhibition in the presence of the mAb51. In vivo, mAb26 significantly diminished ocular pathology intensity in guinea pigs infected with compared to either the mAb51-treated or sham-treated guinea pigs. Our data provide insights that tetanus immunization generates antibodies which induce heterologous chlamydial immunity and promote protection beyond the intended target pathogen.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712554PMC
http://dx.doi.org/10.3390/vaccines8040719DOI Listing

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