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. Author manuscript; available in PMC: 2017 Oct 23.
Published in final edited form as: Sci Immunol. 2017 May 12;2(11):eaam7341. doi: 10.1126/sciimmunol.aam7341

Table 1.

Incorporation of α4β7 and ICAM-1 in a panel of clinical and laboratory HIV-1 and SIV isolates of different clade and coreceptor usage phenotypes grown in activated primary human PBMC. All the clinical isolates were minimally passaged in vitro. The level of virion incorporation was evaluated by measuring the amount of captured p24Gag (or p27Gag for SIV) antigen by immunomagnetic beads armed with anti-ICAM-1/CD54 or anti-α4β7 monoclonal antibodies, and was color-coded in different shades of red (darker to lighter: >1000; 400–1000; 100–400; 0–100 pg/mL).

Virus Strain Clade Coreceptor
usage
Virion
incorporation*
ICAM-1 α4β7

HIV-1 92UG037 A R5 9 406
HIV-1 BaL B R5 275 768
HIV-1 ADA B R5 305 451
HIV-1 JRFL B R5 11 1379
HIV-1 IIIB B X4 64 1385
HIV-1 07USLD B X4 83 658
HIV-1 07USLR B X4 50 1373
HIV-1 92HT599 B R5×4 42 830
HIV-1 93UG065 D X4 414 719
HIV-1 93TH057 E R5 0 457
HIV-1 CMU06 E X4 0 233
HIV-1 97BR019 F R5×4 0 733
SIV smE660.307 n.a. R5 200 508
SIV mac251.745 n.a. R5 235 1499
*

Amount of p24Gag (or p27Gag) antigen (in pg/mL) captured from normalized input virus.