2572. Decreased T-cell Response, But Appropriate Antibody Production to Tetanus Vaccine Among HIV-Exposed Uninfected infants in Botswana
Session: Oral Abstract Session: Pediatric Viral Infections
Saturday, October 6, 2018: 3:00 PM
Room: S 156

Background: In Botswana, more than 10% of HIV-exposed, uninfected infants (HEU) are hospitalized or die in the first 6 months of life, largely due to infectious causes. Vaccine responses can act as a marker of the immune response to infectious antigens. Previous studies of vaccine responses in HEU have had conflicting results. We compared T-cell responses to tetanus and purified protein derivative (PPD), and antibody titers to tetanus, between HEU and HIV-unexposed infants (HUU).

Methods: 443 HIV-infected and 451 HIV-uninfected mothers and their 453 HEU / 457 HUU live-born infants were followed from pregnancy/delivery through 24 months postpartum in a prospective observational study in Botswana (“Tshipidi”). T-cell expression of interferon (IFN)-γ and interleukin (IL)-2 were measured at 6 months using FluoroSpot after stimulation with tetanus toxoid or PPD. Quantitative tetanus toxoid IgG was measured in plasma at 18 months using ELISA. Mean spot-forming units (sfu) per 105 cells and geometric mean antibody titers were compared between HEU and HUU infants who had received 3 doses of tetanus and 1 dose of Bacille Calmette-Guérin (BCG) vaccines by 6 months, and 3 or 4 doses of tetanus vaccine by 18 months.

Results: Peripheral blood mononuclear cells were available at 6 months for 63 HEU and 18 HUU. Plasma was available at 18 months for 39 HEU and 42 HUU. HEU infants had significantly lower IL-2 expression after tetanus stimulation than HUU infants (4.4 vs 16.1 sfu/105 cells, p=0.004; figure), but no difference in IFNγ expression. There were no differences in T-cell responses to PPD between HEU and HUU. There were no differences in tetanus geometric mean antibody titers between HEU and HUU.

Conclusion: In this cohort of infants from Botswana, we found decreased T-cell responses, but not antibody responses, to tetanus toxoid and no differences in T-cell responses to PPD. Cell-mediated immune defects may play a greater role than humoral immune defects in the increased susceptibility to infection among HEU. BCG vaccine produces robust T-helper 1 responses, which may overcome cell-mediated immune defects in HEU.  

Christiana Smith, MD, MS1, Natasha Moraka, BS2, Maryanne Ibrahim, BS3, Sikhulile Moyo, PhD2, Gloria Mayondi, BS2, Betsy Kammerer, PhD4, Jean Leidner, MS5, Simani Gaseitsiwe, PhD2,6, Roger Shapiro, MD, MPH6, Shahin Lockman, MD, MS2,6,7 and Adriana Weinberg, MD, FIDSA1, (1)Pediatric Infectious Diseases, University of Colorado School of Medicine, Aurora, CO, (2)Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana, (3)University of California, Los Angeles, CA, (4)Boston Children’s Hospital, Boston, MA, (5)Goodtables Consulting, Norman, OK, (6)Harvard TH Chan School of Public Health, Boston, MA, (7)Brigham and Women’s Hospital, Boston, MA

Disclosures:

C. Smith, None

N. Moraka, None

M. Ibrahim, None

S. Moyo, None

G. Mayondi, None

B. Kammerer, None

J. Leidner, None

S. Gaseitsiwe, None

R. Shapiro, None

S. Lockman, None

A. Weinberg, None

<< Previous Abstract | Next Abstract

Findings in the abstracts are embargoed until 12:01 a.m. PDT, Wednesday Oct. 3rd with the exception of research findings presented at the IDWeek press conferences.