HIV type 1 superinfection with a dual-tropic virus and rapid progression to AIDS: A case report

被引:29
作者
Gottlieb, Geoffrey S. [1 ]
Nickle, David C.
Jensen, Mark A.
Wong, Kim G.
Kaslow, Richard A.
Shepherd, James C.
Margolick, Joseph B.
Mullins, James I.
机构
[1] Univ Washington, Dept Med, Div Allergy & Infect Dis, Seattle, WA 98195 USA
[2] Univ Georgia, Dept Hlth Adm Biostat & Epidemiol, Athens, GA USA
[3] Univ Georgia, Dept Genet, Athens, GA 30602 USA
[4] Univ Maryland, Dept Med, Div Geograph Med, Baltimore, MD 21201 USA
[5] Univ Washington, Sch Med, Dept Med, Div Allergy & Infect Dis, Seattle, WA 98195 USA
[6] Univ Washington, Sch Med, Dept Microbiol, Div Allergy & Infect Dis, Seattle, WA 98195 USA
[7] Univ Alabama, Dept Epidemiol, Birmingham, AL USA
[8] Univ Alabama, Dept Med, Birmingham, AL 35294 USA
[9] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
[10] Johns Hopkins Univ, Dept Med, Div Infect Dis, Baltimore, MD USA
[11] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD USA
关键词
D O I
10.1086/520024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The occurrence of human immunodeficiency virus type 1 (HIV-1) superinfection has implications for vaccine development and our understanding of HIV pathogenesis and transmission. Methods and Results. We describe a subject from the Multicenter AIDS Cohort Study who was superinfected with a dual-tropic (CXCR4/CCR5-utilizing) HIV-1 subtype B strain between 0.8 and 1.3 years after seroconversion who had rapid progression to AIDS; the subject developed Pneumocystis pneumonia 3.4 years after seroconversion, as well as multiple other opportunistic infections. The superinfecting strain rapidly became the predominant population virus, suggesting that the initial and superinfecting viruses in this individual differed in virulence. However, we found no molecular epidemiological evidence in the HIV database to suggest that this strain had been found in other individuals. In addition, this subject's HIV-1 viral load and pattern of human leukocyte antigen and coreceptor polymorphisms only partially explained his rapid disease progression. Conclusions. Additional studies are needed to determine whether superinfection itself and/or infection with a dual-tropic virus causes rapid disease progression, or whether certain individuals who are innately more susceptible to rapid disease progression also lack the ability to resist the challenge of a second infection. This case appears to support the latter hypothesis.
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收藏
页码:501 / 509
页数:9
相关论文
共 77 条
[61]  
Sheppard HW, 2002, J ACQ IMMUN DEF SYND, V29, P307, DOI 10.1097/00126334-200203010-00013
[62]   HIV drug resistance acquired through superinfection [J].
Smith, DM ;
Wong, JK ;
Hightower, GK ;
Ignacio, CC ;
Koeisch, KK ;
Petropoulos, CJ ;
Richman, DD ;
Little, SJ .
AIDS, 2005, 19 (12) :1251-1256
[63]   HIV superinfection [J].
Smith, DM ;
Richman, DD ;
Little, SJ .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (03) :438-444
[64]   Incidence of HIV superinfection following primary infection [J].
Smith, DM ;
Wong, JK ;
Hightower, GK ;
Ignacio, CC ;
Koelsch, KK ;
Daar, ES ;
Richman, DD ;
Little, SJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 292 (10) :1177-1178
[65]  
SWOFFORD DL, 1999, PAUP 4 PHYLOGENETIC
[66]   HLA class I homozygosity accelerates disease progression in human immunodeficiency virus type I infection [J].
Tang, JM ;
Costello, C ;
Keet, IPM ;
Rivers, C ;
LeBlanc, S ;
Karita, E ;
Allen, S ;
Kaslow, RA .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1999, 15 (04) :317-324
[67]   CCR2 and CCR5 genotypes in HIV type 1-infected adolescents:: Limited contributions to variability in plasma HIV type 1 RNA concentration in the absence of antiretroviral therapy [J].
Tang, JM ;
Wilson, CM ;
Schaen, M ;
Myracle, A ;
Douglas, SD ;
Kaslow, RA .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 2002, 18 (06) :403-412
[68]   Distribution of chemokine receptor CCR2 and CCR5 genotypes and their relative contribution to human immunodeficiency virus type 1 (HIV-1) seroconversion, early HIV-1 RNA concentration in plasma, and later disease progression [J].
Tang, JM ;
Shelton, B ;
Makhatadze, NJ ;
Zhang, Y ;
Schaen, M ;
Louie, LG ;
Goedert, JJ ;
Seaberg, EC ;
Margolick, JB ;
Mellors, J ;
Kaslow, RA .
JOURNAL OF VIROLOGY, 2002, 76 (02) :662-672
[69]  
Theodorou I, 1997, LANCET, V349, P1219
[70]   CLUSTAL-W - IMPROVING THE SENSITIVITY OF PROGRESSIVE MULTIPLE SEQUENCE ALIGNMENT THROUGH SEQUENCE WEIGHTING, POSITION-SPECIFIC GAP PENALTIES AND WEIGHT MATRIX CHOICE [J].
THOMPSON, JD ;
HIGGINS, DG ;
GIBSON, TJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (22) :4673-4680