South African child has controlled HIV off treatment for 8.5 years

A nine-year-old South African child who was diagnosed with HIV infection at one month of age and received HIV treatment for 40 weeks during infancy has suppressed the virus without anti-HIV drugs for eight and a half years, scientists reported today at the 9th IAS Conference on HIV Science (IAS 2017) in Paris, France.  

The child is the third example of an infant who began HIV treatment very soon after birth, stopped treatment after months or years and went on to control HIV infection for a prolonged period. A French child diagnosed at three months of age and treated for somewhere between 5 and 7 years is still controlling HIV off treatment eleven years later. A second child, known as the 'Mississippi Baby', began receiving treatment 30 hours after birth, stayed on treatment for 18 months and then stopped, controlling HIV for 27 months before the virus re-emerged.

The South African child whose case was presented today was treated for a short period after birth as a participant in the CHER study, which compared two early treatment strategies for infants diagnosed with HIV in southern Africa. The child was diagnosed at one month of age, started treatment at two months of age in the group of infants randomised to receive 40 weeks of treatment with lopinavir/ritonavir, zidovudine and lamivudine, and stopped treatment at one year of age. The child had an undetectable viral load below 20 copies/ml by the time of stopping treatment.



The disappearance of signs and symptoms of a disease, usually in response to treatment. The term is often used in relation to cancer, indicating that there is no evidence of disease, although the possibility of cancer remaining in the body cannot be ruled out. In HIV, remission is an alternative term for ‘functional cure’. A sustained ART-free remission would boost the immune system to induce long-term control of HIV, allowing a person living with HIV to maintain an undetectable viral load without daily medication.


The process of viral multiplication or reproduction. Viruses cannot replicate without the machinery and metabolism of cells (human cells, in the case of HIV), which is why viruses infect cells.

immune system

The body's mechanisms for fighting infections and eradicating dysfunctional cells.


A tentative explanation for an observation, phenomenon, or scientific problem. The purpose of a research study is to test whether the hypothesis is true or not.


The ‘HIV reservoir’ is a group of cells that are infected with HIV but have not produced new HIV (latent stage of infection) for many months or years. Latent HIV reservoirs are established during the earliest stage of HIV infection. Although antiretroviral therapy can reduce the level of HIV in the blood to an undetectable level, latent reservoirs of HIV continue to survive (a phenomenon called residual inflammation). Latently infected cells may be reawakened to begin actively reproducing HIV virions if antiretroviral therapy is stopped. 

The child was tested every three months until four years of age to check CD4 cell count, and analysis of stored blood samples now shows that the child maintained an undetectable viral load throughout this follow-up period. Testing at 9.5 years of age shows that HIV is still undetectable and that the number of cells containing HIV DNA – the viral reservoir – has not changed since stopping treatment.

The child exhibits a weak HIV gag-specific CD4 cell response, indicating that the child’s immune system can mount a response to the virus, but lacks CD8 cell responses to HIV. This may mean that very low levels of virus are present but cannot be detected by currently available methods. No replication-competent virus has been isolated using two different methods for culturing virus from potentially infected cells.

Researchers in South Africa and the United States are still trying to explain how the child has controlled HIV. They are careful not to describe the case as a cure; instead, they say, the child’s HIV infection is in remission, controlled by factors that are still to be understood.

“We believe there may have been other factors in addition to early ART that contributed to HIV remission in this child,” said Caroline Tiemessen, Ph.D., whose laboratory at the Centre of HIV and STIs of the National Institute of Communicable Diseases (NICD) in Johannesburg is studying the child’s immune system.

A large study, IMPAACT P1115 is testing the hypothesis that giving ART to HIV-infected newborns beginning within 48 hours of birth may permit long-term control of HIV replication after treatment is stopped, potentially leading to HIV remission. IMPAACT P1115 began in 2014 and has enrolled 42 HIV-infected infants. The first children may become eligible to stop ART in late 2017.


Violari A et al. Viral and host characteristics of a child with perinatal HIV-1 following a prolonged period after ART cessation in the CHER trial. 9th IAS Conference on HIV Science, Paris, abstract TuPDB0106, July 2017.

View the abstract on the conference website.

Download the presentation slides from the conference website.

Watch the webcast of this session on YouTube.