Senior Consultant, Infectious Diseases, Fortis Memorial Research Institute, Gurgaon
Part 2 of 9 in Tuberculosis & HIV - An Insight
How HIV Is Diagnosed: Getting the Testing Window Right
September 6, 2026
A 24-year-old man with multiple sexual partners comes in with fever, swollen lymph nodes and a rash. The reflex differential is a viral illness, strep throat or an allergic reaction, and HIV is the diagnosis doctors most often forget to put on that list. Getting the timing of testing right in a case like this changes whether the infection is caught early or missed entirely.
The Testing Window Nobody Can Shortcut
For the first 14 days after HIV enters the body, no test can reliably detect it. The first marker to appear is the virus itself, picked up by a viral load PCR test from around the second week of infection. From roughly the second to the fourth week, the virus releases a protein called the p24 antigen, which shows up on a blood test but only stays detectable for about two weeks. Only after the fourth week does the immune system produce antibodies that antibody-based tests can detect. Testing too early in this sequence, most commonly ordering an antibody test in the first month, is the single most common reason a genuine infection gets missed.
Why One Positive Test Is Never Enough
A patient walking in with a single positive HIV test result is not yet a confirmed diagnosis. Whether the person is symptomatic, presenting with recurrent fever or an opportunistic infection such as tuberculosis, or asymptomatic and testing because of a known exposure, the same rule applies: three different tests, run either through different methods (ELISA, a rapid card test, a combination test) or targeting different antigens, are needed. Three reactive results confirm HIV. Two reactive results with one indeterminate result are confirmed with a viral load test: a positive viral load confirms the diagnosis, a negative one rules it out. Two clearly negative results out of three end the workup as negative.
The Global Picture Behind Every Local Case
Worldwide, an estimated 84.2 million people have been infected with HIV, of whom roughly a quarter have access to antiretroviral therapy, and about 1.5 million have died of AIDS-related illness. The global target known as 90-90-90 aims for 90 percent of people with HIV to know their status, 90 percent of those to be on treatment, and 90 percent of those on treatment to be taking it with full compliance. The heaviest burden by far sits in the Southeast Asian and African regions, with ten countries, most of them African, accounting for close to half of all new infections worldwide, and Indian settings following close behind.
HIV Infection Is Not the Same as AIDS
HIV can present acutely, as a flu-like illness with high fever, sore throat, cough and swollen lymph nodes, or it can go unnoticed and progress silently into advanced immunodeficiency, which is what AIDS actually is. The distinction matters for how a patient is counselled at diagnosis: having HIV is not the same as having AIDS, and starting antiretroviral therapy promptly, whenever in the course of infection the diagnosis is made, halts that progression rather than simply managing it once it happens.
This guide is based on a live Jivo Masterclass: Dr. Neha Rastogi Panda taught doctors across Africa on March 30, 2025.
FROM THE LIVE Q&A
Dr. Emanuel
Why don't we use the urine LAM test and stool test for all patients?
Dr. Neha Rastogi Panda
The urine lipoarabinomannan (LAM) test is reserved for tuberculosis diagnosis, and it has only been validated for patients with a CD4 count below 100. Below that threshold, a high tuberculosis bacterial burden allows the antigen to wash out into the urine; above it, the test loses sensitivity and specificity, so extrapolating it to every patient isn't supported. On stool testing for other opportunistic infections, a high viral load before treatment changes the normal gut flora, so a stool sample will often show excess normal flora and candida, which makes interpreting it for treatment decisions difficult specifically in HIV patients.
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Frequently Asked Questions
Are there any antiretrovirals that can have prolonged action for up to three or six months?▼
Yes. Cabotegravir, a longer-acting integrase inhibitor, combined with rilpivirine from the non-nucleoside reverse transcriptase inhibitor family, was studied in the TANGO trial and showed viral suppression sustained for close to three months from a single dose. Their half-life runs to about 24 to 26 weeks, so the combination is given as one intramuscular or subcutaneous injection every three months for patients who are already stable on oral therapy, as maintenance rather than as a starting regimen.
At what stage can we diagnose opportunistic infections, and how do we diagnose them?▼
Opportunistic infections can be diagnosed at any stage; the WHO staging system, grade one through four, is built around exactly this, using the infection profile and CD4 level together. Oral thrush, for instance, usually appears at stage two, while reactive generalised lymphadenopathy sits at stage one. Sometimes the opportunistic infection is itself the first clue to an undiagnosed HIV infection, tuberculosis being the clearest example: finding it usually puts the patient at WHO stage three, and a very low viral load and CD4 count below 200 to 250 lets you further risk-stratify from there. Diagnosis runs on three legs: the clinical symptoms and signs, which organ is involved, and targeted sampling, such as testing sputum by GeneXpert for suspected pulmonary tuberculosis, or testing CSF, or serum cryptococcal antigen when CSF isn't accessible, for cryptococcal meningitis.
What are the early signs of HIV?▼
The early signs, known as acute HIV syndrome, look like a flu. Most patients who are symptomatic present with intermittent fever for two to three months, fatigue or weakness, weight loss, loss of appetite, cough, cold, sore throat, more frequent minor illnesses than usual, and loose motions or diarrhoea. This symptom complex over the first month or two is what we call acute HIV syndrome.
Why don't we use the urine LAM test and stool test for all patients?▼
The urine lipoarabinomannan (LAM) test is reserved for tuberculosis diagnosis, and it has only been validated for patients with a CD4 count below 100. Below that threshold, a high tuberculosis bacterial burden allows the antigen to wash out into the urine; above it, the test loses sensitivity and specificity, so extrapolating it to every patient isn't supported. On stool testing for other opportunistic infections, a high viral load before treatment changes the normal gut flora, so a stool sample will often show excess normal flora and candida, which makes interpreting it for treatment decisions difficult specifically in HIV patients.
In This Series: Tuberculosis & HIV - An Insight
- 1.Tuberculosis and HIV
- 2.How HIV Is Diagnosed: Getting the Testing Window Right
- 3.Starting Antiretroviral Therapy: Building the Regimen Around the Patient
- 4.Pre-Exposure Prophylaxis for HIV: Who Qualifies and How Well It Works
- 5.Post-Exposure Prophylaxis: Acting Within 72 Hours of a Possible HIV Exposure
- 6.Tuberculosis and HIV Co-Infection: Why the Two Diseases Compound Each Other
- 7.Preventing Mother-to-Child Transmission of HIV
- 8.When HIV Therapy Appears to Fail: Telling Adherence Problems From Real Failure
- 9.Long-Acting HIV Therapy and the Path Toward a Cure