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Published on: May 21, 2012
Acute chylothorax in children: selective retention of memory T cells and natural killer cells
Jordan S Orange1, Raif S Geha, Francisco A Bonilla
1Division of Immunology, Children's Hospital, Enders Building, 300 Longwood Avenue, Boston, MA 02115, USA.
Insights
Draining chylothorax causes significant IgG and lymphocyte loss, but immune function remains largely intact. Intravenous immunoglobulin (IVIG) did not prevent infections in this small study of hypogammaglobulinemia patients.
Area of Science:
- Immunology
- Pulmonology
Background:
- Hypogammaglobulinemia is a condition characterized by low levels of immunoglobulins.
- Acute chylothorax involves the accumulation of chylous fluid in the pleural space.
Purpose of the Study:
- To evaluate immunodeficiency in patients with hypogammaglobulinemia and draining acute chylothorax.
- To assess humoral and cellular immunity in this patient population.
Main Methods:
- Retrospective review of 8 patients with chylothorax.
- Evaluation of humoral and cellular immunity.
- Analysis of chylous fluid for cellular losses.
Main Results:
- Patients exhibited hypogammaglobulinemia and lymphopenia.
- T cells were decreased, while natural killer cells were increased in peripheral blood.
- In vitro immune responses and vaccine-specific immunity were preserved.
Conclusions:
- Chylothorax leads to IgG and lymphocyte depletion but preserves memory T cells and NK cells.
- Specific antibody levels and T cell function were maintained.
- Intravenous immunoglobulin (IVIG) did not demonstrate clear protection against infections in this cohort.
Objective:
To assess for immunodeficiency in patients with hypogammaglobulinemia in the setting of draining acute chylothorax.
Study Design:
Humoral and cellular immunity was evaluated in 8 patients with chylothorax. Chylous fluid was also analyzed to document cellular losses. Data regarding clinical course and immunologic characteristics were reviewed retrospectively.
Results:
All patients had hypogammaglobulinemia (IgG=179+/-35 mg/dL) as well as lymphopenia (985+/-636 cells/mm(3)). T cells were decreased and natural killer cells increased in peripheral blood. The converse was found in chylous fluid. The ratio of CD3+/CD45RA+ naive: CD3+/CD45RO+ memory T cells was greater in chyle than in peripheral blood. In vitro proliferative responses to antigens and mitogens were similar to control subjects, and previously immunized patients maintained evidence of protective vaccine-specific humoral immunity. To treat hypogammaglobulinemia, patients received intravenous immunoglobulin (IVIG) to maintain IgG within normal range; 6 of 8 patients had serious infections before receiving IVIG compared with 4 of 8 patients during the period of IVIG administration.
Conclusion:
Draining chylothorax resulted in IgG and lymphocyte depletion with preferential retention of memory T cells and natural killer cells in the circulation. Overall, protective-specific antibody levels and T cell function were maintained. IVIG administration did not lead to discernible protection from infectious complications in this small group of patients.
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