Abstract
Background. The immune responses to Pneumocystis jirovecii major surface glycoprotein (Msg) in individuals with human immunodeficiency virus (HIV) infection are poorly understood. Methods. We examined the sequential serologic responses to recombinant Msg carboxyl terminus fragments (MsgC1, MsgC3, MsgC8, and MsgC9) by enzyme-linked immunosorbent assay in a cohort of individuals with HIV infection for the 5.5 years before death and autopsy. Analyses included mean antibody levels by status at death (Pneumocystis pneumonia, P. jirovecii colonization, or neither), factors associated with high antibody levels, and antibody responses before and after active Pneumocystis pneumonia. Results. Patients who died from Pneumocystis pneumonia had higher levels of antibody to MsgC8 than did patients who died from other causes. Previous episode of Pneumocystis pneumonia, geographic location, and age were independent predictors of high levels of anitbodies to most or all Msgs. Failure to take Pneumocystis pneumonia prophylaxis was associated with high levels of antibody to MsgC1. Patients who developed and recovered from active Pneumocystis pneumonia during the study exhibited an increase in serum antibody levels that persisted for months after the infection, whereas patients who developed another acquired immunodeficiency syndrome-defining illness did not. Conclusions. Serum antibodies to Msgs are important markers of P. jirovecii infection in patients with HIV infection and are influenced by host and environmental factors in complex ways.
Original language | English (US) |
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Pages (from-to) | 1335-1344 |
Number of pages | 10 |
Journal | Journal of Infectious Diseases |
Volume | 199 |
Issue number | 9 |
DOIs | |
State | Published - May 1 2009 |
Funding
Financial support: National Institute of Allergy and Infectious Diseases; National Cancer Institute; National Heart, Lung and Blood Institute (grants UO1-AI-35042, 5-MO1-RR-00722 [General Clinical Research Center], UO1-AI-35043, UO1-AI-37984, UO1-AI-35039, UO1-AI-35040, UO1-AI-37613, and UO1-AI-35041); National Institutes of Health (grant M01 RR00425 [General Clinical Research Center] to M.W. and grants R01AI-06492, F33 AI-065207, and R01 HL-090335 to P.D.W.); Medical Research Service, Department of Veterans Affairs (to P.D.W.).
ASJC Scopus subject areas
- Infectious Diseases
- Immunology and Allergy