4.3 Article

Association of Monocyte Migration Marker CD11b With Pulmonary Function in People Living With HIV

Journal

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAI.0000000000002544

Keywords

T cell; monocyte; HIV; lung function; spirometry

Funding

  1. Atlanta CRS [U01-HL146241]
  2. Baltimore CRS [U01-HL146201]
  3. Bronx CRS [U01-HL146204]
  4. Brooklyn CRS [U01-HL146202]
  5. Data Analysis and Coordination Center [U01-HL146193]
  6. ChicagoCook County CRS [U01-HL146245]
  7. Chicago-Northwestern CRS [U01-HL146240]
  8. Connie Wofsy Women's HIV Study, Northern California CRS [U01-HL146242]
  9. Los Angeles CRS [U01-HL146333]
  10. Metropolitan Washington CRS [U01-HL146205]
  11. Miami CRS [U01-HL146203]
  12. Pittsburgh CRS [U01-HL146208]
  13. UAB-MS CRS [U01-HL146192]
  14. UNC CRS [U01-HL146194]
  15. National Heart, Lung, and Blood Institute (NHLBI)
  16. Eunice Kennedy Shriver National Institute Of Child Health and Human Development (NICHD)
  17. National Institute on Aging (NIA)
  18. National Institute Of Dental and Craniofacial Research (NIDCR)
  19. National Institute Of Allergy And Infectious Diseases (NIAID)
  20. National Institute Of Neurological Disorders And Stroke (NINDS)
  21. National Institute Of Mental Health (NIMH)
  22. National Institute On Drug Abuse (NIDA)
  23. National Institute Of Nursing Research (NINR)
  24. National Cancer Institute (NCI)
  25. National Institute on Alcohol Abuse and Alcoholism (NIAAA)
  26. National Institute on Deafness and Other Communication Disorders (NIDCD)
  27. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  28. National Institute on Minority Health and Health Disparities (NIMHD)
  29. UCSF CTSA [UL1-TR000004]
  30. Atlanta CFAR [P30-AI-050409]
  31. UNC CFAR [P30-AI-050410]
  32. UAB CFAR [P30-AI-027767]
  33. IRG Award from the Nancy E. Taylor Foundation for Chronic Diseases, Inc.
  34. [K24HL087713]

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The expression of CD11b(+) on classical monocytes is positively associated with the FEV1/FVC ratio in people living with HIV, especially in those with good CD4 T-cell recovery. This suggests that this specific monocyte subset may play a role in preserving pulmonary function in PLWH.
Background: Maladaptive immune responses contribute to the pathogenesis of many chronic lung diseases. Here, we tested hypotheses that CD4 and CD8 T-cell and monocyte phenotypes are associated with lung function in people living with HIV and those without HIV. Methods: Markers of T cell differentiation, activation, exhaustion and senescence, and markers of monocyte recruitment and migration were quantified in 142 HIV-positive and 73 HIV-negative participants of the Pittsburgh HIV Lung Cohort. All participants underwent lung function testing. Results: CD4 or CD8 T-cell phenotypes were not associated with measures of lung function in HIV-positive or HIV-negative participants after adjustment for multiple comparisons. In HIV-positive participants, however, the percentage of classical monocytes that were CD11b(+) had positive associations at the Bonferroni-adjusted significance threshold of P = 0.05/63 with prebronchodilator and postbronchodilator forced expiratory volume in 1 second (FEV1)/forced vital capacity (FVC) ratio (beta = 0.36; P = 0.00003 and beta = 0.31; P = 0.0003, respectively). In stratified analyses of n = 87 participants with CD4 >= 500 cells/mu L, associations of percentage of classical monocytes that were CD11b(+) with prebronchodilator and postbronchodilator FEV1/FVC ratio were stronger (beta = 0.48 and beta = 0.41, for pre- and post-, respectively) than in the entire HIV-positive study population. Significant associations of monocyte phenotypes were not observed in HIV-negative participants after adjustment for multiple comparisons. Conclusions: CD11b(+) expression on classical monocytes is positively associated with FEV1/FVC ratio in people living with HIV including in those with CD4 T-cell recovery. Given the normal surveillance activity of monocytes, such association suggests this monocyte subset may play a role in preservation of pulmonary function in PLWH.

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