Increase in circulating CD4CD25Foxp3 T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-α

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Increase in circulating CD4CD25Foxp3 T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-α. / Riley, C.H.; Morten Krogh, Jensen; Brimnes, M.K.; Straten, P.T.; Svane, I.M.; Hasselbalch, H.C.; Bjerrum, O.W.

I: Blood, Bind 118, Nr. 8, 25.08.2011, s. 2170-2173.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Riley, CH, Morten Krogh, J, Brimnes, MK, Straten, PT, Svane, IM, Hasselbalch, HC & Bjerrum, OW 2011, 'Increase in circulating CD4CD25Foxp3 T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-α', Blood, bind 118, nr. 8, s. 2170-2173. https://doi.org/10.1182/blood-2011-03-340992

APA

Riley, C. H., Morten Krogh, J., Brimnes, M. K., Straten, P. T., Svane, I. M., Hasselbalch, H. C., & Bjerrum, O. W. (2011). Increase in circulating CD4CD25Foxp3 T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-α. Blood, 118(8), 2170-2173. https://doi.org/10.1182/blood-2011-03-340992

Vancouver

Riley CH, Morten Krogh J, Brimnes MK, Straten PT, Svane IM, Hasselbalch HC o.a. Increase in circulating CD4CD25Foxp3 T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-α. Blood. 2011 aug. 25;118(8):2170-2173. https://doi.org/10.1182/blood-2011-03-340992

Author

Riley, C.H. ; Morten Krogh, Jensen ; Brimnes, M.K. ; Straten, P.T. ; Svane, I.M. ; Hasselbalch, H.C. ; Bjerrum, O.W. / Increase in circulating CD4CD25Foxp3 T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-α. I: Blood. 2011 ; Bind 118, Nr. 8. s. 2170-2173.

Bibtex

@article{718bd6fc1ed44f17a6b2aad5327c6dab,
title = "Increase in circulating CD4CD25Foxp3 T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-α",
abstract = "Recent reports have described complete or major molecular remission in patients with polycythemia vera after long-term treatment with the immunomodulatory agent IFN-α2. Accordingly, there are reasons to believe that the immune system is a key player in eradicating the JAK2 mutated clone in these patients. Foxp3 regulatory T cells play a pivotal role in maintaining immune homeostasis and, importantly, preventing immune reactivity to self-antigens; however, their suppressive activity can compromise an effective antitumor immune response, and high frequencies of regulatory T cells in peripheral blood have been reported in both hematologic and solid cancers. We have analyzed the number, phenotype, and function of circulating CD4 CD25Foxp3 T cells in patients with chronic myeloproliferative neoplasms. Surprisingly, we found a marked expansion of this subset of lymphocytes in patients treated with IFN-α2 (13.0%; 95% confidence interval [CI] 10.8% to 15.2%) compared with healthy donors (6.1%; 95% CI 4.9% to 7.2%), patients with untreated chronic myeloproliferative neoplasms (6.9%; 95% CI 5.8% to 7.4%), or patients treated with hydroxyurea (5.8%; 95% CI 4.3% to 7.4%; P <.0001).",
author = "C.H. Riley and {Morten Krogh}, Jensen and M.K. Brimnes and P.T. Straten and I.M. Svane and H.C. Hasselbalch and O.W. Bjerrum",
year = "2011",
month = aug,
day = "25",
doi = "10.1182/blood-2011-03-340992",
language = "English",
volume = "118",
pages = "2170--2173",
journal = "Blood",
issn = "0006-4971",
publisher = "American Society of Hematology",
number = "8",

}

RIS

TY - JOUR

T1 - Increase in circulating CD4CD25Foxp3 T cells in patients with Philadelphia-negative chronic myeloproliferative neoplasms during treatment with IFN-α

AU - Riley, C.H.

AU - Morten Krogh, Jensen

AU - Brimnes, M.K.

AU - Straten, P.T.

AU - Svane, I.M.

AU - Hasselbalch, H.C.

AU - Bjerrum, O.W.

PY - 2011/8/25

Y1 - 2011/8/25

N2 - Recent reports have described complete or major molecular remission in patients with polycythemia vera after long-term treatment with the immunomodulatory agent IFN-α2. Accordingly, there are reasons to believe that the immune system is a key player in eradicating the JAK2 mutated clone in these patients. Foxp3 regulatory T cells play a pivotal role in maintaining immune homeostasis and, importantly, preventing immune reactivity to self-antigens; however, their suppressive activity can compromise an effective antitumor immune response, and high frequencies of regulatory T cells in peripheral blood have been reported in both hematologic and solid cancers. We have analyzed the number, phenotype, and function of circulating CD4 CD25Foxp3 T cells in patients with chronic myeloproliferative neoplasms. Surprisingly, we found a marked expansion of this subset of lymphocytes in patients treated with IFN-α2 (13.0%; 95% confidence interval [CI] 10.8% to 15.2%) compared with healthy donors (6.1%; 95% CI 4.9% to 7.2%), patients with untreated chronic myeloproliferative neoplasms (6.9%; 95% CI 5.8% to 7.4%), or patients treated with hydroxyurea (5.8%; 95% CI 4.3% to 7.4%; P <.0001).

AB - Recent reports have described complete or major molecular remission in patients with polycythemia vera after long-term treatment with the immunomodulatory agent IFN-α2. Accordingly, there are reasons to believe that the immune system is a key player in eradicating the JAK2 mutated clone in these patients. Foxp3 regulatory T cells play a pivotal role in maintaining immune homeostasis and, importantly, preventing immune reactivity to self-antigens; however, their suppressive activity can compromise an effective antitumor immune response, and high frequencies of regulatory T cells in peripheral blood have been reported in both hematologic and solid cancers. We have analyzed the number, phenotype, and function of circulating CD4 CD25Foxp3 T cells in patients with chronic myeloproliferative neoplasms. Surprisingly, we found a marked expansion of this subset of lymphocytes in patients treated with IFN-α2 (13.0%; 95% confidence interval [CI] 10.8% to 15.2%) compared with healthy donors (6.1%; 95% CI 4.9% to 7.2%), patients with untreated chronic myeloproliferative neoplasms (6.9%; 95% CI 5.8% to 7.4%), or patients treated with hydroxyurea (5.8%; 95% CI 4.3% to 7.4%; P <.0001).

UR - http://www.scopus.com/inward/record.url?scp=80052143261&partnerID=8YFLogxK

U2 - 10.1182/blood-2011-03-340992

DO - 10.1182/blood-2011-03-340992

M3 - Journal article

C2 - 21708889

AN - SCOPUS:80052143261

VL - 118

SP - 2170

EP - 2173

JO - Blood

JF - Blood

SN - 0006-4971

IS - 8

ER -

ID: 48007396