Case Reports in Infectious Diseases

Volume 2014 (2014), Article ID 752312, 3 pages

http://dx.doi.org/10.1155/2014/752312

Case Report

Pediatric HIV Long-Term Nonprogressors

B. H. Rimawi,¹ R. H. Rimawi,² M. Micallef,³ L. Pinckney,⁴ S. L. Fowler,⁵ and T. C. Dixon⁵

¹Department of Obstetrics and Gynecology, Division of Reproductive Infectious Diseases, Division of Maternal Fetal Medicine, Emory University, 550 Peachtree Street NE, Atlanta, GA 30308, USA

²Division of Infectious Diseases and Critical Care, Department of Internal Medicine, Emory University, 550 Peachtree Street NE, Atlanta, GA 30308, USA

³Division of Neonatology, Department of Pediatrics, Medical University of South Carolina, 96 Jonathan Lucas Street, Charleston, SC 29425, USA

⁴Department of Obstetrics and Gynecology, Medical University of South Carolina, 96 Jonathan Lucas Street, Charleston, SC 29425, USA

⁵Division of Infectious Diseases, Department of Pediatrics, Medical University of South Carolina, 96 Jonathan Lucas Street, Charleston, SC 29425, USA

Received 20 May 2014; Accepted 9 August 2014; Published 26 August 2014

Academic Editor: Paola Di Carlo

Copyright © 2014 B. H. Rimawi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Patients infected with HIV are best categorized along a continuum from rapid progressors to HIV long-term nonprogressors. Long-term nonprogressors (LTNPs) are those in which AIDS develop many years after being infected with HIV, often beyond the 10-year mark, and represent 15–20% of the HIV infected patients. Many of these patients are able to control their infection and maintain undetectable viral loads for long periods of time without antiretroviral therapy. After a comprehensive literature search, we found extensive data related to HIV LTNPs in the adult population; however, very limited data was available related to LTNPs within the pediatric population. We present a case of pediatric HIV LTNPs, perinatally infected patient with undetectable viral loads, despite never receiving ART. Although there are not many instances of LTNPs among children, this child may be one, though she had intermittent viremia. She has continued to manifest serologic evidence of infection, with yearly ELISA and western blot positive tests. Based on the viral fitness studies that were performed, this case exemplifies an adolescent LTNP.

1. Introduction

When patients are infected with HIV, their disease process can be best characterized along a continuum from rapid progressors to HIV long-term nonprogressors (LTNPs). Subsets of these patients are characterized as rapid progressors, in which they develop AIDS within a few years, often less than 5 years. In contrast, long-term nonprogressors are those in which AIDS develop many years after being infected with HIV, often beyond the 10-year mark, and represent 15–20% of the HIV infected patients. LTNPs are a subset of long-term nonprogressors, generally referred to as individuals who have contracted the HIV infection but control their infection and maintain undetectable viral loads for long periods of time without antiretroviral therapy [1].

During our literature search, we found extensive data related to HIV LTNPs in the adult population; however, very limited data was available related to LTNPs within the pediatric population. It is important not to confuse pediatric LTNPs with pediatric slow progressors, as the latter is referred to a group of HIV-1-infected pediatric individuals who are homogeneous for route and length of infection and standard of care, thereby having disease progression requiring antiretroviral therapy at some point of their lives. We present a case of pediatric HIV LTNPs, perinatally infected patient with undetectable viral loads, despite never receiving ART.

2. Case Report

A 14-year-old female with a history of HIV acquired via vertical transmission from a noncompliant, advanced AIDS-infected mother presented to our tertiary care hospital. She had no siblings and lived with her mother for the first two years after birth until her mother died of an AIDS-associated infection. Information regarding the HIV status of her biological father was unknown, as this individual was never involved in her care. She missed all her medical appointments while living with her mother. Afterwards, she resided with her maternal grandparents. At that time, she had her first medical evaluation without prior antepartum medical records, where an ELISA and western-blot test were done and came back positive. Her HIV-1 plasma viral load was 1,050-copies/mL and a CD4 count was 2,869 cells per cubic millimeter of blood (CUMM). HIV-1/2 antibody testing confirmed an HIV-1 infection.

She was transferred to an HIV satellite clinic and later to our tertiary infectious disease adolescent clinic. She had never taken ART prior to her MUSC visit. Tables 1 and 2 demonstrate the values of her immunodeficiency panel as well as her HIV-1 viral load since initiation of care at our center. Her repeat HIV-1 plasma RNA viral load was 632-copies/mL with a CD4 count of 2,364/cumm. She was monitored clinically without ART and serial repeat laboratory tests were performed.

Table 1: Clinical laboratory results: CD4/CD8 values.

Date
CD3%
€CD3 absolute #
CD4%
€CD4 absolute #
CD8%
€CD8 absolute #
CD4/CD8 ratio

(: 52–78)
(: 800–3500)
(: 25–48)
(: 400–1200)
(: 9–35)
(: 200–900)
(: 0.9–3.4)

05/07/2009
72
2106
40
1151
29
842
1.4

01/08/2009
74
2049
44
1229
26
713
1.7

08/28/2008
74
1967
43
1152
26
699
1.7

05/29/2008
75
1736
50
1149
22
510
2.3

03/09/2006
73
2240
47
1431
21
649
2.2

11/10/2005
72
2233
44
1359
22
689
2.0

07/21/2005
72
2562
43
1482
26
903
1.6

12/02/2004
74
2806
42
1681
23
928
1.8

03/11/2004
71
3370
51
2186
21
912
2.4

04/14/2003
80
3194
43
1890
23
1041
1.8

12/09/2002
72
3779
43
2153
26
1310
1.6

08/19/2002
75
3976
44
2338
25
1327
1.8

04/15/2002
74
3798
39
2120
24
1328
1.6

01/07/2002
72
3989
45
2517
21
1189
2.1

11/01/2001
62
3699
31
1852
25
1496
1.2

08/09/2001
68
5386
37
2971
23
1868
1.6

05/23/2001
69
4821
31
2686
25
1752
1.3

02/12/2001
70
3706
44
2364
20
1076
2.2

€mm³: cells per cubic millimeter.

: normal reference interval for patient’s age (Medical University of South Carolina).

Table 2: Clinical laboratory results: HIV viral load.

Date
HIV-1 plasma viral load
ELISA/western blot testing

(: <40 copies)
(: negative)

05/07/2009
UD¥
Positive

01/08/2009
UD
Not performed

08/28/2008
UD
Positive

05/29/2007
UD
Positive

03/09/2006
UD
Positive

11/10/2005
UD
Positive

07/21/2005
726
Not performed

12/02/2004
320
Not performed

03/11/2004
476
Positive

04/14/2003
614
Positive

12/09/2002
UD
Not performed

08/19/2002
UD
Not performed

04/15/2002
UD
Not performed

01/07/2002
UD
Positive

10/01/2001
UD
Not performed

07/09/2001
UD
Not performed

04/23/2001
UD
Not performed

02/12/2001
632
Positive

¥UD: undetectable HIV-1 plasma viral load/copies per milliliter.

: normal reference interval (Medical University of South Carolina).

Threshold for detection is any HIV-1 viral load >40 copies/mL.

Method used to quantify HIV-1 plasma RNA viral load: real time PCR.

Her HIV-1 plasma viral load remained undetectable and her viral load remained dramatically unchanged. Repeat ELISA and western blot testing performed on a yearly basis since initial HIV diagnosis have been positive (Table 2). Of note, further investigation was significant for a positive human leukocyte antigen B27 test; however, no deletions or mutations were appreciated. Additional testings for ankylosing spondylitis, reactive arthritis, sacroiliitis, uveitis, and other conditions known to have a positive HLA-B27 antigen test were negative. Proviral HIV tropism testing confirmed a CCR5-tropic (R5) using HIV-1 virus.

Two years later, her viral load rose to 614-copies/mL of plasma. Her viral load remained between undetectable and 727-copies/mL and her CD4 ranged from 1151 to 2186/cumm despite not being initiated on ART. Since 2005, it has remained undetectable without ART. With respect to her overall general clinical course, she has not had any complicating opportunistic infections, hospitalizations, or complications related to HIV. She is a hitherto fit girl, with all the appropriate signs of puberty and sexual development for her age group, including her height and weight.

3. Discussion

Pediatric long-term nonprogressors (LTNPs) are individuals infected with HIV-1 who maintain a suppressed viral load, which refers to either an undetectable viral load (HIV RNA <20 to 75 copies/mL) or a low-detectable HIV-RNA viral load (typically HIV RNA <200 copies/mL), depending on the sensitivity of the HIV RNA assay that is used, despite not being on ART [2]. The clinical relevance of the LTNP classification is not well understood, as some patients remain virologically suppressed, while others have gone on to develop AIDS. LTNPs generally remain at a certain viral load despite not receiving ART [1]. Unlike patients with a “functional” cure, these patients are once known to have detectable HIV-1 RNA viral loads, similar to our index case of 20,000 copies/mL of plasma, and have spontaneously suppressed their viral load and maintained a stable CD4 count without ART influence. Of importance, in comparison to LTNPs, patients with a “functional” cure would test negative for HIV at some point of their care, whereas LTNPs will always have a positive HIV test [2].

After acquisition of HIV, the virus naturally enters into human cells and attach to proteins on that cell. HIV tropism testing allows for knowledge to the type of protein that HIV attaches to. These proteins are the CCR5 and CXCR4, and most HIV infections are caused by the CCR5-using virus; however, as HIV reproduces, it may change from a CCR5-using virus to a CXCR4-using virus. Mutations or deletions in these proteins can account for why an HIV-infected individual rarely progresses to AIDS. Our index patient had a CCR5-tropic using HIV-1 virus.

Different etiologies have been studied which allows long-term nonprogressors to go live without taking ART. These etiologies consist of gene and receptor mutations [3], various mitochondrial DNA types [4], and different human leukocyte antigen (HLA) types, specifically HLA-B27 or HLA-B57 [5]. Perinatally infected children with HIV may acquire the same genes and HLA as their mothers. However, since differences in transcriptional regulation have been observed among different HIV-1 subtypes, the viruses may also be very different. With our index patient, whose mother died secondary to opportunistic infections complicating her advanced AIDS, HLA antigen testing was positive for HLA-B27; however, no deletion or mutation was appreciated.

One question that arises is, was her biological father also HIV-infected? And if so, the possibility of this patient acquiring a mutated HLA B27 gene must be entertained. Unfortunately, her biological father was not involved in her care and his exact presence was unknown; therefore, testing for this was not available and therefore would remain a mystery. Although there are not many instances of LTNPs among children, this child may be one, though she had intermittent viremia. She has continued to manifest serologic evidence of infection, with yearly ELISA and western blot positive tests. Based on the viral fitness studies that were performed, this case exemplifies an adolescent LTNP.

Disclosure

This paper is not under consideration by any other journal.

Conflict of Interests

The authors declare that there is no conflict of interests in the paper, including financial, consultant, institutional, and other relationships that might lead to bias or a conflict of interests.

Authors’ Contribution

All authors have seen and approved the paper and have contributed significantly to the work.

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