Long-term control of CMV retinitis in a patient with idiopathic CD4+ T lymphocytopenia
Abstract Cytomegalovirus (CMV) retinitis with idiopathic CD4+ T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control of CMV retinitis with ICL using interleukin-2 (IL-2) therapy and succeeded in discontinuation of anti-CMV therapy. A 49-year-old Japane...
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Published in | Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy Vol. 19; no. 2; pp. 316 - 320 |
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01.04.2013
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Abstract | Abstract Cytomegalovirus (CMV) retinitis with idiopathic CD4+ T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control of CMV retinitis with ICL using interleukin-2 (IL-2) therapy and succeeded in discontinuation of anti-CMV therapy. A 49-year-old Japanese woman was diagnosed with ICL based on low CD4+ count (72/μl), negative for HIV-1 and -2 antibodies, and absence of any defined immunodeficiency diseases or immunosuppressive therapy. PCR test of the aqueous humor in the right eye was suggestive of CMV retinitis. She was treated with systemic ganciclovir, but after several relapses of CMV retinitis, rhegmatogenous retinal detachment appeared in the right eye and she became blind in that eye. Three years later, she developed CMV retinitis in the left eye. Although she received systemic and focal anti-CMV treatments, the retinitis showed no improvement. Finally, retinal detachment occurred, and she underwent vitrectomy. IL-2 was injected to increase CD4+ counts. Because of hyperpyrexia, blepharedema, central scotoma, and color anomaly, we changed to low-dose IL-2 therapy with no side effects. Finally, we succeeded in increasing the CD4+ count to more than 200/μl after discontinuation of low-dose IL-2 therapy. CMV retinitis never recurred after discontinuation of anti-CMV therapy, with good visual acuity of 20/20 in the left eye. She developed blindness of the first affected right eye, whereas the visual acuity of the left eye remains excellent more than 12 years after the onset of CMV retinitis through the combined use of anti-CMV therapy, IL-2 therapy, and vitrectomy. |
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AbstractList | Cytomegalovirus (CMV) retinitis with idiopathic CD4(+) T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control of CMV retinitis with ICL using interleukin-2 (IL-2) therapy and succeeded in discontinuation of anti-CMV therapy. A 49-year-old Japanese woman was diagnosed with ICL based on low CD4(+) count (72/μl), negative for HIV-1 and -2 antibodies, and absence of any defined immunodeficiency diseases or immunosuppressive therapy. PCR test of the aqueous humor in the right eye was suggestive of CMV retinitis. She was treated with systemic ganciclovir, but after several relapses of CMV retinitis, rhegmatogenous retinal detachment appeared in the right eye and she became blind in that eye. Three years later, she developed CMV retinitis in the left eye. Although she received systemic and focal anti-CMV treatments, the retinitis showed no improvement. Finally, retinal detachment occurred, and she underwent vitrectomy. IL-2 was injected to increase CD4(+) counts. Because of hyperpyrexia, blepharedema, central scotoma, and color anomaly, we changed to low-dose IL-2 therapy with no side effects. Finally, we succeeded in increasing the CD4(+) count to more than 200/μl after discontinuation of low-dose IL-2 therapy. CMV retinitis never recurred after discontinuation of anti-CMV therapy, with good visual acuity of 20/20 in the left eye. She developed blindness of the first affected right eye, whereas the visual acuity of the left eye remains excellent more than 12 years after the onset of CMV retinitis through the combined use of anti-CMV therapy, IL-2 therapy, and vitrectomy. Cytomegalovirus (CMV) retinitis with idiopathic CD4 + T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control of CMV retinitis with ICL using interleukin-2 (IL-2) therapy and succeeded in discontinuation of anti-CMV therapy. A 49-year-old Japanese woman was diagnosed with ICL based on low CD4 + count (72/μl), negative for HIV-1 and -2 antibodies, and absence of any defined immunodeficiency diseases or immunosuppressive therapy. PCR test of the aqueous humor in the right eye was suggestive of CMV retinitis. She was treated with systemic ganciclovir, but after several relapses of CMV retinitis, rhegmatogenous retinal detachment appeared in the right eye and she became blind in that eye. Three years later, she developed CMV retinitis in the left eye. Although she received systemic and focal anti-CMV treatments, the retinitis showed no improvement. Finally, retinal detachment occurred, and she underwent vitrectomy. IL-2 was injected to increase CD4 + counts. Because of hyperpyrexia, blepharedema, central scotoma, and color anomaly, we changed to low-dose IL-2 therapy with no side effects. Finally, we succeeded in increasing the CD4 + count to more than 200/μl after discontinuation of low-dose IL-2 therapy. CMV retinitis never recurred after discontinuation of anti-CMV therapy, with good visual acuity of 20/20 in the left eye. She developed blindness of the first affected right eye, whereas the visual acuity of the left eye remains excellent more than 12 years after the onset of CMV retinitis through the combined use of anti-CMV therapy, IL-2 therapy, and vitrectomy. Abstract Cytomegalovirus (CMV) retinitis with idiopathic CD4+ T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control of CMV retinitis with ICL using interleukin-2 (IL-2) therapy and succeeded in discontinuation of anti-CMV therapy. A 49-year-old Japanese woman was diagnosed with ICL based on low CD4+ count (72/μl), negative for HIV-1 and -2 antibodies, and absence of any defined immunodeficiency diseases or immunosuppressive therapy. PCR test of the aqueous humor in the right eye was suggestive of CMV retinitis. She was treated with systemic ganciclovir, but after several relapses of CMV retinitis, rhegmatogenous retinal detachment appeared in the right eye and she became blind in that eye. Three years later, she developed CMV retinitis in the left eye. Although she received systemic and focal anti-CMV treatments, the retinitis showed no improvement. Finally, retinal detachment occurred, and she underwent vitrectomy. IL-2 was injected to increase CD4+ counts. Because of hyperpyrexia, blepharedema, central scotoma, and color anomaly, we changed to low-dose IL-2 therapy with no side effects. Finally, we succeeded in increasing the CD4+ count to more than 200/μl after discontinuation of low-dose IL-2 therapy. CMV retinitis never recurred after discontinuation of anti-CMV therapy, with good visual acuity of 20/20 in the left eye. She developed blindness of the first affected right eye, whereas the visual acuity of the left eye remains excellent more than 12 years after the onset of CMV retinitis through the combined use of anti-CMV therapy, IL-2 therapy, and vitrectomy. Cytomegalovirus (CMV) retinitis with idiopathic CD4+ T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control of CMV retinitis with ICL using interleukin-2 (IL-2) therapy and succeeded in discontinuation of anti-CMV therapy. A 49-year-old Japanese woman was diagnosed with ICL based on low CD4+ count (72/?l), negative for HIV-1 and -2 antibodies, and absence of any defined immunodeficiency diseases or immunosuppressive therapy. PCR test of the aqueous humor in the right eye was suggestive of CMV retinitis. She was treated with systemic ganciclovir, but after several relapses of CMV retinitis, rhegmatogenous retinal detachment appeared in the right eye and she became blind in that eye. Three years later, she developed CMV retinitis in the left eye. Although she received systemic and focal anti-CMV treatments, the retinitis showed no improvement. Finally, retinal detachment occurred, and she underwent vitrectomy. IL-2 was injected to increase CD4+ counts. Because of hyperpyrexia, blepharedema, central scotoma, and color anomaly, we changed to low-dose IL-2 therapy with no side effects. Finally, we succeeded in increasing the CD4+ count to more than 200/?l after discontinuation of low-dose IL-2 therapy. CMV retinitis never recurred after discontinuation of anti-CMV therapy, with good visual acuity of 20/20 in the left eye. She developed blindness of the first affected right eye, whereas the visual acuity of the left eye remains excellent more than 12 years after the onset of CMV retinitis through the combined use of anti-CMV therapy, IL-2 therapy, and vitrectomy. |
Author | Tachikawa, Natsuo Fujino, Yujiro Inamochi, Kazuya Yashiro, Shigeko Oka, Shinichi |
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Cites_doi | 10.1046/j.1365-2249.1999.00886.x 10.1016/j.ajo.2005.07.017 10.1006/clim.2001.5016 10.1182/blood-2007-12-127878 10.1073/pnas.89.16.7831 10.1001/jama.1992.03490100046010 10.2500/aap.2008.29.3143 10.1016/S0171-2985(00)80068-6 10.1093/clinids/18.6.1012 10.1111/j.1365-2249.2009.03910.x 10.1177/112067210801800525 10.1056/NEJM199302113280601 |
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Keywords | Cytomegalovirus retinitis Vitrectomy IL-2 CD4 + T lymphocytopenia T lymphocytopenia CD4 |
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Unexpected opportunistic infections and CD4 + T-lymphocytopenia without HIV infection publication-title: N Engl J Med doi: 10.1056/NEJM199302113280601 contributor: fullname: Smith – volume: 268 start-page: 1252 year: 1992 ident: 10.1007/s10156-012-0464-x_bib0010 article-title: CD4 + T-lymphocytopenia in persons without evident HIV infection: United States publication-title: JAMA doi: 10.1001/jama.1992.03490100046010 contributor: fullname: Kessler – volume: 7 start-page: 424 year: 1988 ident: 10.1007/s10156-012-0464-x_bib0065 article-title: Transient decrease in IL-2-responsive lymphocytes 24 hours after initiation of continuous IL-2 infusion in cancer patients publication-title: J Biol Response Mod contributor: fullname: Weil-Hillman – volume: 202 start-page: 204 year: 2000 ident: 10.1007/s10156-012-0464-x_bib0040 article-title: Successful IL-2 therapy for relapsing herpes zoster infection in a patient with idiopathic CD4+ T lymphocytopenia publication-title: Immunobiology doi: 10.1016/S0171-2985(00)80068-6 contributor: fullname: Warnatz |
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Snippet | Abstract Cytomegalovirus (CMV) retinitis with idiopathic CD4+ T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term... Cytomegalovirus (CMV) retinitis with idiopathic CD4 + T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control of... Cytomegalovirus (CMV) retinitis with idiopathic CD4(+) T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control... Cytomegalovirus (CMV) retinitis with idiopathic CD4+ T lymphocytopenia (ICL) is rare and difficult to control. We report a first case for long-term control of... |
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SubjectTerms | Antiviral Agents - therapeutic use Case Report Cytomegalovirus Cytomegalovirus Retinitis - blood Cytomegalovirus Retinitis - drug therapy Female Ganciclovir - therapeutic use Hematology, Oncology and Palliative Medicine Human immunodeficiency virus 1 Humans Infectious Diseases Interleukin-2 - therapeutic use Medical Microbiology Medicine Medicine & Public Health Middle Aged Retinal Detachment - surgery T-Lymphocytopenia, Idiopathic CD4-Positive - complications T-Lymphocytopenia, Idiopathic CD4-Positive - drug therapy Virology Vitrectomy |
Title | Long-term control of CMV retinitis in a patient with idiopathic CD4+ T lymphocytopenia |
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