The effect of acute infectious illnesses on plasma human immunodeficiency virus (HIV) type 1 load and the expression of serologic markers of immune activation among HIV-infected adults. 1998

M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

The effect of acute coinfections on plasma human immunodeficiency virus (HIV) load and immune activation markers was evaluated. Thirty-two HIV-infected persons were prospectively enrolled; 18 had pre-illness, acute, and follow-up specimens. Plasma HIV RNA levels were determined by reverse transcriptase-polymerase chain reaction, and serum levels of activation markers, including tumor necrosis factor (TNF)-alpha, soluble (s) TNF receptors (R)-I and -II, interleukin (IL)-2, IL-6, IL-10, sIL-2R, sCD4, and sCD8, were assessed by commercial ELISAs. Median plasma HIV load increased 7. 8-fold during illness (P=.001) and decreased 1.5-fold (P=.01) during convalescence (median, 15 days). Significant virus load reductions were limited to subjects with clinical recovery. By regression analysis, changes in plasma HIV RNA were significantly associated with changes in sTNFR-I, sTNFR-II, and sIL-2R. Increased HIV replication during acute coinfections is associated with in vivo immune activation, which underscores the need to prevent and promptly treat intercurrent illnesses.

UI MeSH Term Description Entries
D011446 Prospective Studies Observation of a population for a sufficient number of persons over a sufficient number of years to generate incidence or mortality rates subsequent to the selection of the study group. Prospective Study,Studies, Prospective,Study, Prospective
D003141 Communicable Diseases An illness caused by an infectious agent or its toxins that occurs through the direct or indirect transmission of the infectious agent or its products from an infected individual or via an animal, vector or the inanimate environment to a susceptible animal or human host. Infectious Diseases,Communicable Disease,Disease, Communicable,Disease, Infectious,Diseases, Communicable,Diseases, Infectious,Infectious Disease
D003289 Convalescence The period of recovery following an illness. Convalescences
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000208 Acute Disease Disease having a short and relatively severe course. Acute Diseases,Disease, Acute,Diseases, Acute
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D012367 RNA, Viral Ribonucleic acid that makes up the genetic material of viruses. Viral RNA
D013997 Time Factors Elements of limited time intervals, contributing to particular results or situations. Time Series,Factor, Time,Time Factor
D014409 Tumor Necrosis Factor-alpha Serum glycoprotein produced by activated MACROPHAGES and other mammalian MONONUCLEAR LEUKOCYTES. It has necrotizing activity against tumor cell lines and increases ability to reject tumor transplants. Also known as TNF-alpha, it is only 30% homologous to TNF-beta (LYMPHOTOXIN), but they share TNF RECEPTORS. Cachectin,TNF-alpha,Tumor Necrosis Factor Ligand Superfamily Member 2,Cachectin-Tumor Necrosis Factor,TNF Superfamily, Member 2,TNFalpha,Tumor Necrosis Factor,Cachectin Tumor Necrosis Factor,Tumor Necrosis Factor alpha
D015375 Receptors, Interleukin-2 Receptors present on activated T-LYMPHOCYTES and B-LYMPHOCYTES that are specific for INTERLEUKIN-2 and play an important role in LYMPHOCYTE ACTIVATION. They are heterotrimeric proteins consisting of the INTERLEUKIN-2 RECEPTOR ALPHA SUBUNIT, the INTERLEUKIN-2 RECEPTOR BETA SUBUNIT, and the INTERLEUKIN RECEPTOR COMMON GAMMA-CHAIN. IL-2 Receptors,Interleukin-2 Receptor,Interleukin-2 Receptors,Receptors, IL-2,Receptors, T-Cell Growth Factor,T-Cell Growth Factor Receptors,IL-2 Receptor,IL2 Receptor,IL2 Receptors,Interleukin 2 Receptor,Receptor, TCGF,T-Cell Growth Factor Receptor,TCGF Receptor,TCGF Receptors,IL 2 Receptor,IL 2 Receptors,Interleukin 2 Receptors,Receptor, IL-2,Receptor, IL2,Receptor, Interleukin 2,Receptor, Interleukin-2,Receptors, IL 2,Receptors, IL2,Receptors, Interleukin 2,Receptors, T Cell Growth Factor,Receptors, TCGF,T Cell Growth Factor Receptor,T Cell Growth Factor Receptors

Related Publications

M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
May 2001, The Journal of infectious diseases,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
March 2012, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
August 2001, The Journal of infectious diseases,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
September 1993, The Journal of infectious diseases,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
December 2008, The Indian journal of medical research,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
September 2000, AIDS research and human retroviruses,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
September 1997, The Journal of infectious diseases,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
January 2010, PloS one,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
August 2014, Journal of virology,
M S Sulkowski, and R E Chaisson, and C L Karp, and R D Moore, and J B Margolick, and T C Quinn
August 2000, The Journal of infectious diseases,
Copied contents to your clipboard!