Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: May 9, 2026

Development of Cell-type specific anti-HIV gp120 aptamers for siRNA delivery
13:47

Development of Cell-type specific anti-HIV gp120 aptamers for siRNA delivery

Published on: June 23, 2011

Multiantibody strategies for HIV.

Andrew Hiatt1, Larry Zeitlin, Kevin J Whaley

  • 1Mapp Biopharmaceutical Inc., 6160 Lusk Boulevard, C104, San Diego, CA 92121, USA. andy.hiatt@mappbio.com

Clinical & Developmental Immunology
|July 11, 2013
PubMed
Summary

Viruses like HIV can evade neutralizing antibodies (nAbs) by exploiting robust immune responses. This review explores viral immune evasion and discusses multi-antibody therapy to overcome this challenge.

Related Concept Videos

Retrovirus Life Cycles01:10

Retrovirus Life Cycles

Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Osteosarcoma in the Setting of Genetically Confirmed <i>IFITM5-</i>Related Osteogenesis Imperfecta.

Case reports in pathology·2026
Same author

Avidity and variable domain spacing strongly influence the therapeutic potency of bispecific antibodies against Crimean-Congo hemorrhagic fever virus.

mBio·2025
Same author

Antibody-dependent complement-mediated sperm cytotoxicity in the endocervix is a dominant contraceptive mechanism of ZB-06 vaginal film.

Fertility and sterility·2024
Same author

Impact of mAb-FcRn affinity on IgG transcytosis across human well-differentiated airway epithelium.

Frontiers in immunology·2024
Same author

A Longitudinal Analysis of Memory Immune Responses in Convalescent Crimean-Congo Hemorrhagic Fever Survivors in Uganda.

The Journal of infectious diseases·2024
Same author

Crimean-Congo hemorrhagic fever survivors elicit protective non-neutralizing antibodies that target 11 overlapping regions on glycoprotein GP38.

Cell reports·2024

Area of Science:

  • Immunology
  • Virology
  • Vaccinology

Background:

  • Effective vaccination relies on immune system responsiveness to antigens.
  • Neutralizing antibodies (nAbs) are crucial for combating pathogen infectivity.
  • Some viruses, such as HIV, have evolved mechanisms to evade nAbs.

Purpose of the Study:

  • To review viral immune evasion strategies stemming from robust immune responses.
  • To present a rationale for using multi-antibody therapy against viral evasion.
  • To outline advancements in monoclonal antibody (mAb) development and approval.

Main Methods:

  • Literature review of viral immune evasion mechanisms.
  • Analysis of immune response exploitation by viruses.
  • Discussion of therapeutic strategies involving multiple antibodies.

Main Results:

  • Viruses can adapt to circumvent neutralizing antibody responses.
  • Robust immune responses can paradoxically facilitate viral immune evasion.
  • Progress in monoclonal antibody technology offers potential therapeutic avenues.

Conclusions:

  • Viral immune evasion is a significant challenge in vaccination and infection control.
  • Multi-antibody therapies show promise in overcoming viral evasion.
  • Advancements in monoclonal antibody production and regulation support their clinical application.

More Related Videos

Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice
06:07

Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice

Published on: October 6, 2022

Related Experiment Videos

Last Updated: May 9, 2026

Development of Cell-type specific anti-HIV gp120 aptamers for siRNA delivery
13:47

Development of Cell-type specific anti-HIV gp120 aptamers for siRNA delivery

Published on: June 23, 2011

Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice
06:07

Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice

Published on: October 6, 2022