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Updated: Aug 6, 2026

A Restriction Enzyme Based Cloning Method to Assess the In vitro Replication Capacity of HIV-1 Subtype C Gag-MJ4 Chimeric Viruses
Published on: August 31, 2014
HIV vaccine development
1Vaccine and Prevention Research, Division of AIDS, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892-7628, USA. pj7p@nih.gov
Abstract:
Optimism prevails that a safe and at least partially effective HIV vaccine will be identified within this decade. Public, philanthropic and private sector efforts to expand the development pipeline and to indude candidates based on diverse HIV subtypes have proved successful. Yet both scientific and logistical obstacles remain. No vaccine candidate yet induces broadly neutralizing antibodies. The type, level, location and durability of immune responses necessary for protection remain unknown. For those vaccines that may not prevent HIV infection but control replication and prevent disease, the issue of transmissibility must be addressed. Other challenges indude improving infrastructure and research capabilities and establishing or strengthening regulatory agencies in developing countries. Another key issue is ensuring access to successful vaccines, which will require large-scale manufacturing and development of policies and processes to distribute vaccine to those most in need.
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