PKPeter S. Kim

Peter S. Kim

*This is an algorithmically generated author record based on publicly available information.

Research Subjects

Research Interests


Peter S. Kim has a total of 3 co-authors. Here are the top co-authors by number of shared publications:

  • Christine Sizemore

    Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland

    1 shared publication
  • Mamodikoe Makhene

    Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland

    1 shared publication
  • Richard Hafner

    Division of AIDS

    1 shared publication

Latest Publications

  • Open Access

    Viewpoint: Challenges and Opportunities in Tuberculosis Research

    by Peter S. Kim, Mamodikoe Makhene, Christine Sizemore, Richard Hafner

    Partially fueled by the human immunodeficiency virus (HIV) pandemic, tuberculosis is the second-leading cause of infectious diseases–associated mortality globally and the leading cause of death among those infected with HIV. In 2010, there were an estimated 8.8 million incident cases of tuberculosis and approximately 1.5 million deaths attributed to tuberculosis. Increased public heath efforts have been effective in decreasing the overall prevalence and mortality associated with this disease, but declines in incidence rates have been outpaced by global population growth, such that absolute incidence rates have not declined as fast as previously expected [1]. Commensurate with increased public recognition of the importance of tuberculosis to global health in the mid-1990s, biomedical research for tuberculosis has increased both in the United States and internationally. Although tools to conduct modern biomedical research involving tuberculosis have only been available for a little over a decade, this research has resulted in several successes, including promising new vaccines to protect against tuberculosis in the highest-risk populations, diagnostic candidates to improve the accuracy and speed of diagnosing all forms of tuberculosis, and new drug candidates with the potential for improved treatment and chemoprevention for drug-sensitive and drug-resistant tuberculosis.