Limited HIV Infection of Central Memory and Stem Cell Memory CD4+ T Cells Is Associated with Lack of Progression in Viremic Individuals

被引:72
|
作者
Klatt, Nichole R. [1 ,2 ]
Bosinger, Steven E. [3 ,4 ]
Peck, Melicent [5 ]
Richert-Spuhler, Laura E. [1 ]
Heigele, Anke [6 ]
Gile, Jillian P. [1 ]
Patel, Nirav [3 ,4 ]
Taaffe, Jessica [3 ,4 ]
Julg, Boris [7 ]
Camerini, David [8 ]
Torti, Carlo [9 ]
Martin, Jeffrey N. [5 ]
Deeks, Steven G. [5 ]
Sinclair, Elizabeth [5 ]
Hecht, Frederick M. [5 ]
Lederman, Michael M. [10 ]
Paiardini, Mirko [3 ,4 ]
Kirchhoff, Frank [6 ]
Brenchley, Jason M. [2 ]
Hunt, Peter W. [5 ]
Silvestri, Guido [3 ,4 ]
机构
[1] Univ Washington, Dept Pharmaceut, Washington Natl Primate Res Ctr, Seattle, WA 98195 USA
[2] NIAID, Mol Microbiol Lab, NIH, Bethesda, MD 20892 USA
[3] Emory Univ, Yerkes Primate Res Ctr, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[4] Emory Univ, Dept Pathol, Atlanta, GA 30322 USA
[5] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[6] Univ Ulm, Med Ctr, Inst Mol Virol, D-89069 Ulm, Germany
[7] Ragon Inst MGH MIT & Harvard, Boston, MA USA
[8] Univ Calif Irvine, Inst Immunol, Irvine, CA USA
[9] Univ Brescia, Inst Infect & Trop Dis, Brescia, Italy
[10] Case Western Reserve Univ, Div Infect Dis, Univ Hosp Case Med Ctr, Cleveland, OH 44106 USA
关键词
IMMUNODEFICIENCY-VIRUS CONTROLLERS; IMMUNE ACTIVATION; SIV INFECTION; SOOTY MANGABEY; PERSISTENCE; RESPONSES; DISEASE; PROLIFERATION; BIOMARKERS; RESERVOIR;
D O I
10.1371/journal.ppat.1004345
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A rare subset of HIV-infected individuals, designated viremic non-progressors (VNP), remain asymptomatic and maintain normal levels of CD4+ T-cells despite persistently high viremia. To identify mechanisms potentially responsible for the VNP phenotype, we compared VNPs (average >9 years of HIV infection) to HIV-infected individuals who have similar CD4+ T-cell counts and viral load, but who are likely to progress if left untreated ("putative progressors'', PP), thus avoiding the confounding effect of differences related to substantial CD4+ T cell depletion. We found that VNPs, compared to PPs, had preserved levels of CD4+ stem cell memory cells (TSCM (p<0.0001), which was associated with decreased HIV infection of these cells in VNPs (r = -0.649, p = 0.019). In addition, VNPs had decreased HIV infection in CD4+ central memory (T-CM) cells (p = 0.035), and the total number of TCM cells was associated with increased proliferation of memory CD4+ T cells (r = 0.733, p = 0.01). Our results suggest that, in HIV-infected VNPs, decreased infection of CD4+ T-CM and T-SCM, cells are involved in preservation of CD4+ T cell homeostasis and lack of disease progression despite high viremia.
引用
下载
收藏
页数:13
相关论文
共 50 条
  • [31] Acute rotavirus infection is associated with the induction of circulating memory CD4+ T cell subsets
    Chikondi Malamba-Banda
    Chimwemwe Mhango
    Prisca Benedicto-Matambo
    Jonathan J. Mandolo
    End Chinyama
    Orpha Kumwenda
    Kayla G. Barnes
    Nigel A. Cunliffe
    Miren Iturriza-Gomara
    Kondwani C. Jambo
    Khuzwayo C. Jere
    Scientific Reports, 13
  • [32] Progressive CD4+ central-memory T cell decline results in CD4+ effector-memory insufficiency and overt disease in chronic SIV infection
    Okoye, Afam
    Meier-Schellersheim, Martin
    Brenchley, Jason M.
    Hagen, Shoko I.
    Walker, Joshua M.
    Rohankhedkar, Mukta
    Lum, Richard
    Edgar, John B.
    Planer, Shannon L.
    Legasse, Alfred
    Sylwester, Andrew W.
    Piatak, Michael, Jr.
    Lifson, Jeffrey D.
    Maino, Vernon C.
    Sodora, Donald L.
    Douek, Daniel C.
    Axthelm, Michael K.
    Grossman, Zvi
    Picker, Louis J.
    JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (09): : 2171 - 2185
  • [33] HIV-1-specific memory CD4+ T cells are phenotypically less mature than cytomegalovirus-specific memory CD4+ T cells
    Yue, FY
    Kovacs, CM
    Dimayuga, RC
    Parks, P
    Ostrowski, MA
    JOURNAL OF IMMUNOLOGY, 2004, 172 (04): : 2476 - 2486
  • [34] Persistence and function of central and effector memory CD4+ T cells following infection with a gastrointestinal helminth
    Zaph, Colby
    Rook, Kathryn A.
    Goldschmidt, Michael
    Mohrs, Markus
    Scott, Phillip
    Artis, David
    JOURNAL OF IMMUNOLOGY, 2006, 177 (01): : 511 - 518
  • [35] Requirement of B Cells for Generating CD4+ T Cell Memory
    Whitmire, Jason K.
    Asano, Mary S.
    Kaech, Susan M.
    Sarkar, Surojit
    Hannum, Lynn G.
    Shlomchik, Mark J.
    Ahmed, Rafi
    JOURNAL OF IMMUNOLOGY, 2009, 182 (04): : 1868 - 1876
  • [36] Naive and Memory CD4+ T Cells in HIV Eradication and Immunization Reply
    Lewis, Joanna
    Walker, A. Sarah
    Castro, Hannah
    De Rossi, Anita
    Gibb, Diana M.
    Giaquinto, Carlo
    Klein, Nigel
    Callard, Robin
    JOURNAL OF INFECTIOUS DISEASES, 2012, 206 (04): : 618 - 618
  • [37] Human adipose tissue as a reservoir for memory CD4+ T cells and HIV
    Couturier, Jacob
    Suliburk, James W.
    Brown, Jeremy M.
    Luke, David J.
    Agarwal, Neeti
    Yu, Xiaoying
    Chi Nguyen
    Iyer, Dinakar
    Kozinetz, Claudia A.
    Overbeek, Paul A.
    Metzker, Michael L.
    Balasubramanyam, Ashok
    Lewis, Dorothy E.
    AIDS, 2015, 29 (06) : 667 - 674
  • [38] Central Memory CD4+ T Cells Dominate the Normal Cerebrospinal Fluid
    de Graaf, Marieke T.
    Smitt, Peter A. E. Sillevis
    Luitwieler, Ronald L.
    van Velzen, Chris
    van den Broek, Patricia D. M.
    Kraan, Jaco
    Gratama, Jan W.
    CYTOMETRY PART B-CLINICAL CYTOMETRY, 2011, 80B (01) : 43 - 50
  • [39] Quantifying Susceptibility of CD4+ Stem Memory T-Cells to Infection by Laboratory Adapted and Clinical HIV-1 Strains
    Flynn, Jacqueline K.
    Paukovics, Geza
    Cashin, Kieran
    Borm, Katharina
    Ellett, Anne
    Roche, Michael
    Jakobsen, Martin R.
    Churchill, Melissa J.
    Gorry, Paul R.
    VIRUSES-BASEL, 2014, 6 (02): : 709 - 726
  • [40] Vaccination Expands Antigen-Specific CD4+ Memory T Cells and Mobilizes Bystander Central Memory T Cells
    Li Causi, Eleonora
    Parikh, Suraj C.
    Chudley, Lindsey
    Layfield, David M.
    Ottensmeier, Christian H.
    Stevenson, Freda K.
    Di Genova, Gianfranco
    PLOS ONE, 2015, 10 (09):