Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis

Nitin J. Karandikar, Steven H. Kroft, Subramanian Yegappan, Beverly B. Rogers, Victor M. Aquino, Kyung-Mi Lee, Vinay Kumar, F. Javier Guenaga, Elaine S. Jaffe, Daniel C. Douek, Robert W. McKenna

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Familial hemophagocytic lymphohistiocytosis (FHL) is an inherited, fatal disorder of infancy. We report here a 17-day-old female infant who presented with high fever, hepatosplenomegaly, hypertriglyceridemia, hypofibrinogenemia, thrombocytopenia, and liver failure. Leukocytosis was detected with circulating "atypical" lymphoid cells. Flow cytometric studies revealed expanded subpopulations of CD8+ T cells with unusual immunophenotypic features, including a subset that lacked CD5 expression. A liver biopsy showed hemophagocytic lymphohistiocytosis with exuberant infiltrates of CD8+ T cells that lacked perforin. Mutational studies revealed a 666C→A (H222Q) missense mutation in the perforin gene. T-cell receptor studies on flow-sorted T-cell subpopulations revealed no evidence of monoclonality. Analysis of T-cell receptor excision circle levels indicated long proliferative history in the aberrant CD8+ T-cell subsets. This case provides an instructive example of uncontrolled reactive proliferation of CD8+ T cells in FHL, resulting in atypical morphology and unusual immunophenotypic features that might suggest malignancy in other clinical settings.

Original languageEnglish
Pages (from-to)2007-2009
Number of pages3
JournalBlood
Volume104
Issue number7
DOIs
Publication statusPublished - 2004 Oct 1

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Hemophagocytic Lymphohistiocytosis
T-cells
T-Lymphocytes
Perforin
T-Cell Antigen Receptor
Liver
Hypertriglyceridemia
Leukocytosis
Liver Failure
T-Lymphocyte Subsets
Missense Mutation
Thrombocytopenia
Biopsy
Fever
History
Lymphocytes
Genes
Neoplasms

ASJC Scopus subject areas

  • Hematology

Cite this

Karandikar, N. J., Kroft, S. H., Yegappan, S., Rogers, B. B., Aquino, V. M., Lee, K-M., ... McKenna, R. W. (2004). Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis. Blood, 104(7), 2007-2009. https://doi.org/10.1182/blood-2004-04-1431

Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis. / Karandikar, Nitin J.; Kroft, Steven H.; Yegappan, Subramanian; Rogers, Beverly B.; Aquino, Victor M.; Lee, Kyung-Mi; Kumar, Vinay; Guenaga, F. Javier; Jaffe, Elaine S.; Douek, Daniel C.; McKenna, Robert W.

In: Blood, Vol. 104, No. 7, 01.10.2004, p. 2007-2009.

Research output: Contribution to journalArticle

Karandikar, NJ, Kroft, SH, Yegappan, S, Rogers, BB, Aquino, VM, Lee, K-M, Kumar, V, Guenaga, FJ, Jaffe, ES, Douek, DC & McKenna, RW 2004, 'Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis', Blood, vol. 104, no. 7, pp. 2007-2009. https://doi.org/10.1182/blood-2004-04-1431
Karandikar NJ, Kroft SH, Yegappan S, Rogers BB, Aquino VM, Lee K-M et al. Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis. Blood. 2004 Oct 1;104(7):2007-2009. https://doi.org/10.1182/blood-2004-04-1431
Karandikar, Nitin J. ; Kroft, Steven H. ; Yegappan, Subramanian ; Rogers, Beverly B. ; Aquino, Victor M. ; Lee, Kyung-Mi ; Kumar, Vinay ; Guenaga, F. Javier ; Jaffe, Elaine S. ; Douek, Daniel C. ; McKenna, Robert W. / Unusual immunophenotype of CD8+ T cells in familial hemophagocytic lymphohistiocytosis. In: Blood. 2004 ; Vol. 104, No. 7. pp. 2007-2009.
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