TY - JOUR
T1 - Anatomical loci of HIV-associated immune activation and association with viraemia
AU - Iyengar, Sujatha
AU - Chin, Bennett
AU - Margolick, Joseph B.
AU - Sabundayo, Beulah P.
AU - Schwartz, David H.
N1 - Funding Information:
We thank Arlette Lindsay for care of the patients, Susan Langan for data management and analysis, Charlamaine Henson and Thomas Quinn for plasma HIV RNA measurements, Stacey Meyerer and Jessica Noyes for processing of blood samples, and Arron Pighee and Janice Boring for coordination of study visits. This study was supported by NIH grants AI 41532, R21-AI 44725, and a Center for AIDS Research developmental grant award to SI (CFAR P30-AI42855). DS was the recipient of a grant from the Alternatives Research Development Fund.
PY - 2003/9/20
Y1 - 2003/9/20
N2 - Background: Lymphocyte activation, associated with vaccination or infection, can be measured by positron emission tomography (PET). We investigated the ability of PET to detect and measure magnitude of lymph-node activation among asymptomatic HIV-1-infected individuals. Methods: Initially we assessed PET response in eight HIV-1-uninfected individuals who had received licensed killed influenza vaccine. In an urban teaching hospital, we recruited 12 patients recently infected with HIV-1 (<18 months since seroconversion) and 11 chronic long-term HIV-1 patients who had stable viraemia by RT-PCR (non-progressors). After injection with fluorine-18-labelled fluorodeoxyglucose, patients underwent PET. We correlated summed PET signal from nodes with viral load by linear regression on log-transformed values. Findings: Node activation was more localised after vaccination than after HIV-1 infection. In early and chronic HIV-1 disease, node activation was greater in cervical and axillary than in inguinal and iliac chains (p<0·0001), and summed PET signal correlated with viraemia across a 4 log range (r2=0·98, p<0·0001). Non-progressors had small numbers of persistently active nodes, most of which were surgically accessible. Interpretation: The anatomical restriction we noted may reflect microenvironmental niche selection, and tight correlation of PET signal with viraemia suggests target-cell activation determines steady-state viral replication.
AB - Background: Lymphocyte activation, associated with vaccination or infection, can be measured by positron emission tomography (PET). We investigated the ability of PET to detect and measure magnitude of lymph-node activation among asymptomatic HIV-1-infected individuals. Methods: Initially we assessed PET response in eight HIV-1-uninfected individuals who had received licensed killed influenza vaccine. In an urban teaching hospital, we recruited 12 patients recently infected with HIV-1 (<18 months since seroconversion) and 11 chronic long-term HIV-1 patients who had stable viraemia by RT-PCR (non-progressors). After injection with fluorine-18-labelled fluorodeoxyglucose, patients underwent PET. We correlated summed PET signal from nodes with viral load by linear regression on log-transformed values. Findings: Node activation was more localised after vaccination than after HIV-1 infection. In early and chronic HIV-1 disease, node activation was greater in cervical and axillary than in inguinal and iliac chains (p<0·0001), and summed PET signal correlated with viraemia across a 4 log range (r2=0·98, p<0·0001). Non-progressors had small numbers of persistently active nodes, most of which were surgically accessible. Interpretation: The anatomical restriction we noted may reflect microenvironmental niche selection, and tight correlation of PET signal with viraemia suggests target-cell activation determines steady-state viral replication.
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U2 - 10.1016/S0140-6736(03)14363-2
DO - 10.1016/S0140-6736(03)14363-2
M3 - Article
C2 - 14511927
AN - SCOPUS:0141831931
SN - 0140-6736
VL - 362
SP - 945
EP - 950
JO - Lancet
JF - Lancet
IS - 9388
ER -