Table 1. Patient characteristics of elite suppressors, chronic progressors, and acutely infected individuals.
Patient | Year of diagnosis | Sampling date | Duration of infectiona | Plasma viral load (RNA copies/ml) | CD4 count (cells/µl) |
Elite Suppressors | |||||
ES2 | 1986 | 5/04 | 18 years | <50 | 383 |
ES3 | 1991 | 3/04 | 13 years | <50 | 677 |
ES4 | 1996 | 8/04 | 8 years | <50 | 837 |
ES7 | 1994 | 1/05 | 11 years | <50 | 1,125 |
ES8 | 2003 | 6/04, 9/04 | 1 year | <50 | 458 |
ES9 | 1999 | 3/04, 8/04 | 5 years | <50 | 800 |
ES10 | 2002 | 3/04 | 2 years | <50 | 900 |
Chronic Progressors | |||||
C61 | 1999 | 9/04 | 5 years | 19,100 | 1,261 |
C62 | 1998 | 9/04 | 6 years | 33,300 | 481 |
C93 | 2001 | 3/05 | 4 years | 47,270 | 402 |
C94 | 1999 | 2/05 | 6 years | 22,898 | 351 |
C96 | 2001 | 3/05 | 4 years | 12,500 | 400 |
C98 | 2004 | 3/05 | 1 year | 17,838 | 426 |
C109 | 2002 | 5/05 | 3 years | 61,000 | 222 |
Acute Infection | |||||
502 | – | – | 19 days | 31,622,777 | 306 |
503 | – | – | 17 days | 588,844 | 531 |
504 | – | – | 32 days | 2,691,535 | 152 |
506 | – | – | 43 days | 467,735 | 341 |
508 | – | – | 26 days | 389,045 | 266 |
510 | – | – | 16 days | 1,584,893 | 581 |
512 | – | – | 25 days | 3,388,442 | 745 |
514 | – | – | 26 days | 676,083 | 291 |
516 | – | – | 51 days | 295,121 | 371 |
517 | – | – | 38 days | 87,096 | 588 |
518 | – | – | 15 days | 21,379,621 | 226 |
519 | – | – | 22 days | 1,819,701 | 322 |
520 | – | – | 40 days | 257,040 | 512 |
522 | – | – | 21 days | 3,235,937 | 583 |
523 | – | – | 28 days | 173,780 | 273 |
526 | – | – | 26 days | 100,000 | 205 |
527 | – | – | 21 days | 134,896 | 538 |
528 | – | – | 16 days | 12,022,644 | 438 |
529 | – | – | 19 days | 28,840,315 | 537 |
530 | – | – | 30 days | 6,456,542 | 469 |
Time of infection expressed in approximate years for ES and CP patients from diagnosis to sampling. Time of infection for acute infection samples estimated by 14 days after the onset of acute seroconversion symptoms or identification of high risk transmission event, and sampling was conducted <4 weeks post-presentation and initiation of HAART.