Skip to main content

Table 1 Clinical characteristics of CRF01_AE subtype HIV-1-infected individuals

From: A longitudinal analysis of immune escapes from HLA-B*13-restricted T-cell responses at early stage of CRF01_AE subtype HIV-1 infection and implications for vaccine design

PID

HLA class I

Early

3 monthsd

1 year

Set pointa

HLA-A

HLA-B

HLA-C

dpi

CD4 (cells/μL)

VL (copies/mL)

dpi

CD4 (cells/μL)

VL (copies/mL)

dpi

CD4 (cells/μL)

VL (copies/mL)

320829

A24 A24

B13 B15

C03 C03

51b

531

5.42

120b

653

5.44

352b

616

5.43

5.44

320018

A02 A30

B13 B13

C06 C07

34b

464

5.33

58bc

293

5.18

330bc

281

5.08

5.08

320853

A01 A30

B13 B40

C03 C06

43b

351

3.98

ND

ND

ND

226bc

141

4.58

4.67

321145

A11 A30

B13 B38

C06 C07

38b

472

5.85

138b

642

5.26

318b

525

4.79

4.62

320019

A02 A30

B13 B46

C01 C06

46b

163

4.46

58bc

163

4.61

381bc

411

4.77

4.50

321221

A11 A30

B13 B38

C06 C07

37b

549

5.32

85

548

4.70

393b

559

5.08

4.53

320088

A02 A11

B13 B13

C02 C03

53

ND

4.82

62bc

330

4.07

327bc

321

4.86

4.43

300471

A02 A30

B13 B35

C04 C06

134

269

4.23

139b

262

4.23

360bc

277

4.29

4.20

325020

A02 A24

B13 B40

C03 C08

ND

ND

ND

59bc

638

3.29

309bc

551

4.06

3.58

325029

A30 A30

B13 B13

C05 C06

27

429

5.40

83b

572

4.46

337b

573

3.10

3.59

320571

A02 A30

B13 B54

C01 C06

ND

ND

ND

131c

353

4.71

335c

373

4.63

4.50

320006

A02 A02

B13 B13

C03 C14

47

407

4.24

108c

500

3.95

395

306

3.71

3.74

320135

A02 A32

B13 B44

C03 C04

46b

685

3.77

63bc

590

4.37

427bc

564

3.75

3.75

440230

A02 A30

B13 B46

C01 C06

71

343

2.02

78b

333

4.59

371b

318

2.20

2.05

  1. VL, viral load; dpi, days post-infection; ND, not detected
  2. a Average viral load (at least three time points) from 120 days to 1 year of infection
  3. b Deep-sequencing was undertaken at the indicated number of days post-HIV-1 infection
  4. c An interferon-gamma (IFN-γ) enzyme-linked immunospot (ELISPOT) assay was performed for patients at the indicated number of days post-HIV-1 infection
  5. d Available samples at the time point closest to 3 months of HIV-1 infection