Development of a Highly Protective Combination Monoclonal Antibody Therapy against Chikungunya Virus

  • Pankaj Pal*
  • , Kimberly A. Dowd
  • , James D. Brien
  • , Melissa A. Edeling
  • , Sergey Gorlatov
  • , Syd Johnson
  • , Iris Lee
  • , Wataru Akahata
  • , Gary J. Nabel
  • , Mareike K. S. Richter
  • , Jolanda M. Smit
  • , Daved H. Fremont
  • , Theodore C. Pierson
  • , Mark T. Heise
  • , Michael S. Diamond
  • *Corresponding author voor dit werk

OnderzoeksoutputAcademicpeer review

243 Citaten (Scopus)
488 Downloads (Pure)

Samenvatting

Chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus that causes global epidemics of a debilitating polyarthritis in humans. As there is a pressing need for the development of therapeutic agents, we screened 230 new mouse anti-CHIKV monoclonal antibodies (MAbs) for their ability to inhibit infection of all three CHIKV genotypes. Four of 36 neutralizing MAbs (CHK-102, CHK-152, CHK-166, and CHK-263) provided complete protection against lethality as prophylaxis in highly susceptible immunocompromised mice lacking the type I IFN receptor (Ifnar(-/-)) and mapped to distinct epitopes on the E1 and E2 structural proteins. CHK-152, the most protective MAb, was humanized, shown to block viral fusion, and require Fc effector function for optimal activity in vivo. In post-exposure therapeutic trials, administration of a single dose of a combination of two neutralizing MAbs (CHK-102+CHK-152 or CHK-166+CHK-152) limited the development of resistance and protected immunocompromised mice against disease when given 24 to 36 hours before CHIKV-induced death. Selected pairs of highly neutralizing MAbs may be a promising treatment option for CHIKV in humans.

Originele taal-2English
Artikelnummere1003312
Aantal pagina's16
TijdschriftPLoS Pathogens
Volume9
Nummer van het tijdschrift4
DOI's
StatusPublished - 18-apr.-2013

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