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Clinical and Diagnostic Laboratory Immunology, November 2005, p. 1331-1333, Vol. 12, No. 11
1071-412X/05/$08.00+0     doi:10.1128/CDLI.12.11.1331-1333.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Immunoglobulin G({kappa}) [IgG({kappa})] and IgG({lambda}) Paraproteinemia in a Child with AIDS and Response to Highly Active Antiretroviral Therapy

Filiz Odabasi Seeborg,1* Hannah Gay,2 Lorenz M. Schmiege III,3 David Bernard,4 and William T. Shearer1

Section of Allergy & Immunology, Texas Children's Hospital and Baylor College of Medicine,1 Department of Pathology, Baylor College of Medicine, Houston, Texas 77030,3 Pediatric Infectious Disease Division, University of Mississippi Medical Center, Jackson, Mississippi 39213,2 Department of Pathology, The Methodist Hospital, Houston, Texas 77030, and Weill Medical College of Cornell University, New York, New York 100214

Received 5 August 2004/ Returned for modification 29 November 2004/ Accepted 13 September 2005


   ABSTRACT
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We report an 8-year-old boy with AIDS, extremely elevated serum immunoglobulin G (IgG) concentration and IgG kappa [IgG({kappa})] and IgG lambda [IgG({lambda})] paraproteinemia. This paraproteinemia partially responded to highly active antiretroviral therapy. This case emphasizes the importance of controlling B-cell activation.


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B-cell activation during human immunodeficiency virus type 1 (HIV-1) infection is a specific response to HIV-1 determinants (1, 2, 3). This activation, which can be either monoclonal or oligoclonal, can result in hypergammaglobulinemia, a common finding in AIDS (12). Moreover, oligoclonal immunoglobulin (Ig) bands can be observed in asymptomatic HIV-1-seropositive individuals (14).

We report an 8-year-old HIV-1-seropositive boy with AIDS and an extremely elevated serum IgG level (nephelometry) (University of Mississippi, Jackson, MS). Two months prior to his birth, his mother was diagnosed with HIV-1 infection. Despite maternal treatment and patient prophylaxis with zidovudine (ZDV), the patient's HIV-1 DNA PCR test (Amplicor HIV-1 Monitor Test; Roche Diagnostic Systems, Branchburg, NJ) was positive at 4 and 6 weeks of age. His initial CD4 cell assessment (flow cytometry) (Epics XL/MCL, Miami, FL) was 59%, with a count of 3,754/mm3 at 6 weeks of age. The patient remained well until developing Streptococcus pneumoniae sepsis at 7 months of age. Despite CD4 counts above 1,000/mm3, his serum Ig levels became diffusely elevated (Table 1). This initial episode of sepsis was followed by recurrent clinical problems, including pneumococcal septicemia, chronic otitis media with perforation, mastoiditis, parotitis, febrile seizures, possible miliary tuberculosis, severe lymphoid interstitial pneumonitis, hepatosplenomegaly, and failure to thrive.


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  		TABLE 1. Comparison of serum immunoglobulin levels, peripheral blood CD4 cells, and plasma HIV-RNA levels in a child with paraproteinemiaa

 
Over the years, the patient has been treated with several combinations of antiretroviral agents. However, due to poor compliance, his HIV-1 viral load remained persistently elevated (Table 1). Whether our patient acquired ZDV-resistant HIV-1 from his mother is unknown, because viral genotyping was not available when he was born. When the patient was 6 years of age, his mother requested that his antiretroviral medications be discontinued. At 6.5 years of age, the CD4 cell percentage was 10% (184 cells/mm3), CD8 cell percentage was 54%, and HIV-1 viral load was 68,207 RNA copies/ml. Laboratory studies revealed total protein of 13.4 g/dl and an elevated serum total IgG concentration of 8 g/dl. A bone marrow biopsy revealed normal results, and tests for autoantibodies proved negative. At 7.5 years of age, the child's HIV-RNA levels were extremely elevated at 380,000 copies/ml. After counseling about the possibility of malignancy developing in their child, his parents agreed to initiate the highly active antiretroviral therapy (HAART) program of ZDV, lamivudine, and lopinavir. Over the next 6 months, the child's HIV-1 RNA levels, serum Ig, and total protein levels (data not shown) decreased, and the CD4 cell percentage and count improved (Table 1). Serum protein electrophoresis (SPE) and immunofixation were performed prior to and after the HAART.

The initial (prior to HAART treatment at age 7.5 years old) SPE (Hydrasys LC; Sebia, Norcross, GA) demonstrated diffusely increased gammaglobulins with three discrete bands that immunofixed as two monoclonal IgG({kappa}) bands and a single monoclonal IgG({lambda}) band (Fig. 1). These findings were consistent with an oligoclonal Ig immune response. The cerebrospinal fluid protein level was normal, and oligoclonal IgG bands were not present. Urine protein (130 mg/24 h) electrophoresis showed three monoclonal IgG({kappa}) bands and one monoclonal IgG({lambda}) band (data not shown). The follow-up (after HAART at 8 years of age) SPE demonstrated a striking reduction in the intensity of the oligoclonal bands, and one IgG({kappa}) band had disappeared (Fig. 1).



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  		FIG. 1. Immunofixation of (A) the patient's serum prior to treatment (age, 7.5 years old) and (B) the patient's serum after treatment (age, 8 years old). Prior to treatment, the serum contained three IgG monoclonal bands: two monoclonal IgG({kappa}) bands and one monoclonal IgG({lambda}) band. After treatment, one of the previously identified monoclonal IgG({kappa}) bands is no longer identifiable. The letters at the top of the figure represent the following: ELP, electrophoresis; G, IgG; A, IgA; M, IgM; K, kappa light chain; L, lambda light chain.

 
We present the clinical and laboratory findings of an HIV-1-seropositive child with paraproteinemia consisting of oligoclonal IgG bands. Oligoclonal Ig in HIV-seropositive patients has been previously described as mixed {kappa} and {lambda} light chains (8, 11), single heavy chains (7, 11), and single {kappa} chains (13), although IgA({kappa}) and IgM({kappa}) bands have also been identified (15, 16). Hypergammaglobulinemia, a well-known consequence of HIV-1 infection resulting from B-cell activation, is often associated with paraproteins and may be observed at any stage of the disease (6, 8, 11, 14). IgG bands in the serum of HIV-1-seropositive subjects are known to be specific for viral determinants (9). Although hypergammaglobulinemia frequently occurs in HIV-1 infection, a striking feature of this case was the magnitude of the IgG paraproteinemia and the appearance of IgG chains in the urine. The child's serum oligoclonal IgG band pattern was similar to that of previously reported adult patients (2, 6, 13). HIV-1-seropositive patients with monoclonal or oligoclonal bands are more likely to develop non-Hodgkin lymphoma than those without paraproteinemia (4). Moreover, atypical plasma cells, plasma cell aggregates, and plasma cell hyperplasia of the bone marrow may develop even in the absence of plasma cell neoplasia in HIV-1-seropositive patients (16). Some HIV-1-seropositive patients present with transient paraproteinemias, while others have persistent paraproteins with or without true plasma cell malignancies (5). Furthermore, Epstein-Barr virus has been associated with the development of non-Hodgkin’s lymphoma in patients with AIDS (1). The bone marrow examination of our patient did not, however, reveal any abnormalities as to the percentage, number, or morphology of plasma cells.

Potent antiretroviral therapy in HIV-1-seropositive patients with paraproteinemia decreases the hyperactivation of B cells, which normalizes total IgG concentrations. In addition, the viral suppression by antiretroviral therapy results in a diminished HIV-1-virus-specific antibody response (10). When HAART treatment was successfully maintained for 6 months in our patient, the paraproteinemia decreased, and one of the IgG({kappa}) oligoclonal bands became undetectable (Fig. 1). Although we did not measure the serum IgG level just prior to the adherent antiretroviral therapy, the greatly reduced gamma region on the SPE supports our claim that the serum IgG level declined secondary to the antiretroviral therapy. Currently, the patient has been adherent to his antiretroviral therapy. His most recent CD4% is up to 32%, and viral load is undetectable.

In conclusion, this case report adds new information that sustained activation of B lymphocytes plays a crucial role in the immune dysfunction in pediatric HIV-1 infection. Although this patient and some reported adult patients (9) did not develop lymphoma over a 3-year period, we believe that long-term follow-up protocols should be developed to determine the outcome of children with this condition and to determine if lymphoma develops as an ultimate pathogenetic event.


   ACKNOWLEDGMENTS
 
We were supported by National Institutes of Health grants and contracts AI 27551, AI 36211, HD 41983, RR 0188, HL 72705, and 202PICL05; the Pediatric Research and Education Fund, Baylor College of Medicine; and the David Fund, Pediatric AIDS Fund, and Immunology Research Fund, Texas Children's Hospital.


   FOOTNOTES
 
* Corresponding author. Mailing address: Texas Children's Hospital, 6621 Fannin Street (MC; FC330.01), Houston, TX 77030. Phone: (832) 824-1274. Fax: (832) 825-7131. E-mail: fodabasi{at}hotmail.com. Back


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Clinical and Diagnostic Laboratory Immunology, November 2005, p. 1331-1333, Vol. 12, No. 11
1071-412X/05/$08.00+0     doi:10.1128/CDLI.12.11.1331-1333.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




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