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Author Notes:

Miwako Kobayashi, MD, MPH, Division of Bacterial Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Atlanta, GA 30329, MS H24-6 (e-mail: ydk3@cdc.gov)

We thank everyone in the Active Bacterial Core surveillance (ABCs) areas who was involved in the surveillance and maintenance of the system. We also thank the laboratorians and technicians who isolate the ABCs pathogens and make it possible to track these infections and the surveillance and laboratory personnel at the CDC for their careful work characterizing the isolates. We would like to acknowledge the following members of the ABCs team and others for their contributions at the study sites:

Susan Brooks, Pam Daily-Kirley, Maria Rosales, Joelle Nadle, Katie Wymore (CA); Derek Evans, Carmen Marquez, and Daniel Wurm (CT); Wendy Baughman, Stephanie Thomas, and Amy Tunali (GA); Terresa Carter, Shannon Seopaul (MD); Brenda Jewell, Lori Triden, Megan Sulkulski, Kathy Como-Sabetti, Richard Danila, Ruth Lynfield, Paula Snippes, and Anita Glennen (MN); Kathy M. Angeles, Sarah A. Khanlian, Lisa Butler, Robert Mansmann, Emily Hancock, Karen Scherzinger, Gaby Keener, Joanne Keefe, S. Elizabeth Racz, Isaac Armistead, Chad Smelser, Salina Torres, Joseph Bareta, Brooke Doman, Megin Nichols, Chelsea McMullen, and Jeremy Espinoza (NM); Heather Jamieson, Tasha Martin (OR); Tiffanie Markus, Brenda Barnes, and Katie Dyer (TN).

W.S. served as a consultant for VBI Vaccines. L.H.H served as a consultant for GSK, Merck, Pfizer, and Sanofi Pasteur. The remaining authors have no conflicts of interest to disclose.

Subjects:

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • Infectious Diseases
  • 13-valent pneumococcal conjugate vaccine
  • invasive pneumococcal disease
  • indirect effects
  • direct effects
  • HIV infection
  • STREPTOCOCCUS-PNEUMONIAE INFECTIONS
  • POLYSACCHARIDE VACCINE
  • ANTIRETROVIRAL THERAPY
  • ADVISORY-COMMITTEE
  • RACIAL DISPARITIES
  • RISK-FACTORS
  • ERA
  • RECOMMENDATIONS
  • PREVENTION
  • RESPONSES

Impact of 13-Valent Pneumococcal Conjugate Vaccine on Invasive Pneumococcal Disease Among Adults With HIV-United States, 2008-2018

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Journal Title:

JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES

Volume:

Volume 90, Number 1

Publisher:

, Pages 6-14

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Background:People with HIV (PWH) are at increased risk for invasive pneumococcal disease (IPD). Thirteen-valent pneumococcal conjugate vaccine (PCV13) was recommended for use in US children in 2010 and for PWH aged 19 years or older in 2012. We evaluated the population-level impact of PCV13 on IPD among PWH and non-PWH aged 19 years or older.Methods:We identified IPD cases from 2008 to 2018 through the Active Bacterial Core surveillance platform. We estimated IPD incidence using the National HIV Surveillance System and US Census Bureau data. We measured percent changes in IPD incidence from 2008 to 2009 to 2017-2018 by HIV status, age group, and vaccine serotype group, including serotypes in recently licensed 15-valent (PCV15) and 20-valent (PCV20) PCVs.Results:In 2008-2009 and 2017-2018, 8.4% (552/6548) and 8.0% (416/5169) of adult IPD cases were among PWH, respectively. Compared with non-PWH, a larger proportion of IPD cases among PWH were in adults aged 19-64 years (94.7%-97.4% vs. 56.0%-60.1%) and non-Hispanic Black people (62.5%-73.0% vs. 16.7%-19.2%). Overall and PCV13-type IPD incidence in PWH declined by 40.3% (95% confidence interval: -47.7 to -32.3) and 72.5% (95% confidence interval: -78.8 to -65.6), respectively. In 2017-2018, IPD incidence was 16.8 (overall) and 12.6 (PCV13 type) times higher in PWH compared with non-PWH; PCV13, PCV15/non-PCV13, and PCV20/non-PCV15 serotypes comprised 21.5%, 11.2%, and 16.5% of IPD in PWH, respectively.Conclusions:Despite reductions post-PCV13 introduction, IPD incidence among PWH remained substantially higher than among non-PWH. Higher-valent PCVs provide opportunities to reduce remaining IPD burden in PWH.
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