Table 2. HIV in blood cells.
Sample | Date | Lab | Measure | Input | Assay | Detection Limit | False Positive Rate1 | Result |
PBMC | 5/31/11 | NIH | HIV DNA | 30×106 cells | qPCR for LTR [19] | 0.5–2.6 copy/µg | 0/72 (<1.4%) | ND2 |
PBMC | 7/5/11 | SFVA/UCSF | HIV DNA | 106 cells | qPCR for LTR [24], [56] | 1–2 copy/reaction [56] | 1/130 (0.8%) | 1 of 10 wells equivocal |
PBMC | 11/17/11 | Johns Hopkins | HIV DNA | 106 cells | qPCR for Gag [25] | 1 copy/reaction | ND (≤1 in 106) | |
PBMC | 8/1/11 | UCSD | HIV DNA | 106 cells | Digital droplet PCR for Pol [26] | 0.52 copy/106 cells | 7/29 (24%) | ND (≤1 in 106) |
PBMC (sorted) | 2/29/12 | Vaccine Research Center | HIV DNA | 6.7×104 CCR5+ cells | Fluorescence- assisted clonal amplification of Env | 1 copy/reaction | ND | |
7.6×106 CCR5− non-T cells | ND | |||||||
3.5×106 CCR5− CD4+ T cells | ND | |||||||
2.1×106 other CCR5− T cells | ND | |||||||
PBMC | 5/31/11 | NIH | HIV RNA | 10×106 cells | Roche Ampliprep [19] | 1–2 copy/ml | 1/179 (0.6%) | ND (≤1 in 107) |
PBMC | 7/5/11 | SFVA/UCSF | HIV RNA | 106 cells | qRT-PCR for LTR [24], [56] | 1–2 copy/reaction [56] | 0/83 (<1.2%) | ND (≤1 in 106) |
PBMC | 6/20/11 | BSRI | HIV RNA | 3×106 cells | TMA [22] | 1 copy/ml [22] | 6/3515 (0.2%) | ND (≤1 in 3×106) |
PBMC (sorted) | 2/29/12 | Vaccine Research Center | HIV RNA | 6.8×104 CCR5+ cells | RNA sequencing | 1 read/sample | ND | |
8.6×106 CCR5− non-T cells | ND | |||||||
3.4×106 CCR5− CD4+ T cells | ND | |||||||
4.2×106 other CCR5− T cells | ND | |||||||
Peripheral CD4+T cells | 5/31/11 | NIH | Replication compent HIV (IUPM) | 1.4×109 cells | Co-culture [27] | ND (≤1 IU/109 cells) | ||
Resting peripheral CD4+ T cells | 11/17/11 | Johns Hopkins | Replication compent HIV (IUPM) | 33×106 cells | Co-culture [28] | ND (≤1 IU/107 cells) |
Historical, as determined from the number of positive wells out of all wells containing samples from HIV- subjects/donors that had been processed and run along with positive samples.
ND = not detected.