Case Report
HIV-2 Infections from a Tertiary Care Hospital in India-A Case Report
Malhotra S*, Dhundial R, Bhatia NJK, Chauhan A and Duggal N
Corresponding Author: Dr. Shalini Malhotra, Dept. of Microbiology, PGIMER and associated Dr RMLH, New Delhi, India
Received: January 24, 2018; Revised: June 12, 2018; Accepted: February 28, 2018
Citation: Malhotra S, Dhundial R, Bhatia NJK, Chauhan A & Duggal N. (2018) HIV-2 Infections from a Tertiary Care Hospital in India-A Case Report. J Clin Trials Res, 1(1): 1-3.
Copyrights: ©2018 Malhotra S, Dhundial R, Bhatia NJK, Chauhan A & Duggal N. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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HIV-1 has spread globally, whereas HIV-2 has mostly remained limited to West Africa. India is one of the countries where a dual epidemic of HIV 1 & 2 is occurring. There are several reports indicating presence of HIV-2 infection in India. First case of HIV-2 from India was reported from Mumbai, in 1991. Since then it has been identified from geographically diverse states, yet reliable data regarding HIV-2 epidemiology in India is still lacking. According to some studies, the prevalence of HIV in various parts of India is different. It is particularly high in the western and the southern parts. In western India, HIV-2 and dual infections with HIV-1 and HIV-2 have been reported since early nineties and in South India in late nineties. The following is a report of a case of HIV-2 infection from a tertiary care hospital in North India.


Keywords: HIV- 2, Human Immunodeficiency Virus, Prevalence



Approximately 2.1 million people are currently living with HIV AIDS in India [1]. In 1986, the first case of HIV infection in India was detected among sex workers in Chennai [2]. In the same year, HIV-2 was isolated from AIDS patients in West Africa [3]. The first evidence of HIV-2 infection in India was provided in 1991 [4]. Since then it has been sporadically reported from various states of India. HIV-2 appears to be transmitted principally by sexual contact, with prostitutes being the well-studied group. The virus can also be spread by blood transfusion of infected blood. Compared to HIV-1, transmission of HIV-2 virus from an infected mother to her child seems to be less frequent. However, cases of transmission from an infected woman to her foetus have been reported among women who had primary HIV- 2 infection during their pregnancy [5]. The prevalence rate of HIV-2 infection in India is not available so far. The following is a report of HIV-2 infection from Delhi in North India.


A 45 year old laborer presented to an integrated counseling and testing centre (ICTC) as a direct walk-in for HIV testing in July 2016 with unexplained chronic diarrhea for longer than one month and generalized weakness. The patient was a resident of Delhi and stayed with his spouse. The patient gave a history of frequent contacts with commercial sex workers (CSW).

Following the guidelines of the National AIDS Control Organization (NACO), after informed consent and pre-test counseling, his blood sample was tested for HIV using a rapid test (CombAids, J Mitra, Delhi) following manufacturer’s instructions. Test was reactive for HIV, following which two more rapid tests (SD Bioline; Aids scan Tri-spot) were carried out on the same sample (one test was able to differentiate between HIV-1 and 2). The sample was reactive on all three tests and was further confirmed by Western blot. The patient was found to be HIV-2 positive and was registered with the anti-retroviral therapy (ART) Centre.

Since the patient gave a history of regular unprotected sex with his spouse, we suggested the wife to be tested for HIV. She was found to be negative for HIV as per NACO guidelines.

His CD4 T-cell count was 266 (22%) cells/mm3 and did not have any other significant laboratory abnormality. His other autoimmune profile was normal.



Although HIV-2 infection is mostly confined to West African countries it has been identified in other continents following sexual contact with foreigners with a history of frequent contact with CSWs, as in our case [6]. These CSWs provide a bridge for transferring HIV-2 infection from high prevalence regions, such as West African countries, to low prevalence countries, such as India.

Sequential serological surveys from a Hospital population in Tamil Nadu during 1993-97 and 2000-01 showed a stable HIV-2 prevalence over time, at 2.47% of all HIV diagnoses [7]. The frequency of HIV-2 in a blood donor population at a tertiary referral hospital in Southern India between the period 1998-2007 was also similar at 2.8% of all HIV diagnoses [1.3% HIV-2 and 1.5% HIV 1 & 2 dual infections] [8]. Various studies from South and West India has reported that HIV-2 prevalence ranges from 0.3 – 2.1%. [5,9,10] Murugan and Amburajan observed a prevalence of 0.29% of HIV-2 in south Tamil Nadu, and Solomon et, al. reported a prevalence rate of 0.9% with HIV-2 among urban population [11,12]. There are various reports of HIV 2 infection from South India but data from North India is much limited.

It was seen that more discordant couples exist with HIV-2 infection than HIV-1 infection as was seen in our case and his spouse in spite of having regular unprotected sex. Reason being that compared to HIV-1, those with HIV-2 are less infectious early in the course of infection [13,14].

No guidelines regarding the clinical treatment and care of patients infected with HIV-2 are available yet. As we know that HIV-2 virus is intrinsically resistant to NNRTI and to enfluvirtide and some protease inhibitors are also ineffective, the treatment options are limited. It is also not known whether any potential benefits would outweigh the possible adverse effects of treatment.

Estimation of HIV-2 viral load assays is another major problem with no commercially available assay. Viral load assays used for HIV-1 are not reliable for monitoring HIV-2. Therefore, monitoring the treatment response of patients infected with HIV-2 is more difficult than monitoring people infected with HIV-1. There is need to standardize, validate, and commercialize simple, low-cost HIV-2 viral load assays. The only option available to monitor the response to treatment for HIV-2 infection is by secondary parameters like CD4+T-cell counts and other indicators of immune system deterioration such as weight loss, oral candidiasis, unexplained fever, and the appearance of a new AIDS defining illness.

To determine the most effective treatment for HIV-2, more efforts in terms of research are needed. We need the exact prevalence and incidence of HIV-2 infection in our country to establish proper guidelines and different regimens for management of HIV-2. Otherwise, it is possible to have serious resistant strains of HIV-2 which will possibly pose a problem in our country in the future as the present regimen given in government anti-retroviral therapy (ART) centers is not highly active anti-retroviral therapy (HAART).

In conclusion, continued surveillance is needed to monitor for and develop special guidelines for HIV-2 in the Indian population. Physicians involved in screening for HIV need to have a high index of suspicion in patients with risk factors for HIV-2 infection, to appropriately diagnose and treat the disease since these patients develop AIDS related symptoms late due to delayed progression. Guidelines should be created for HIV testing of spouses with HIV-2 infection to diagnose and treat the disease, since these cases have inefficient transmission.

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13.    Andersson S, Norrgren H, Silva ZD, et al. (2000) Pasma viral load in HIV-1 and HIV-2 singly and dually infected individuals in Guinea-Bissau, West Africa significantly lower plasma virus set point in HIV-2 infection than in HIV-1 infection. Arch Intern Med 160: 3286-3293.

14.    Popper SJ, Sarr AD, Gue‘Ye-ndiaye A, Mboup S, Essex ME, et al. (2000) Low plasma human immunodeficiency virus type 2 viral load is independent of proviral load: low virus production in vivo. J Virol 74: 1554-1557.