Proteomic patterns predict acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation.

Standard

Proteomic patterns predict acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation. / Weissinger, Eva M; Schiffer, Eric; Hertenstein, Bernd; Ferrara, James L; Holler, Ernst; Stadler, Michael; Kolb, Hans-Jochem; Zander, Axel R.; Zürbig, Petra; Kellmann, Markus; Ganser, Arnold.

in: BLOOD, Jahrgang 109, Nr. 12, 12, 2007, S. 5511-5519.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Weissinger, EM, Schiffer, E, Hertenstein, B, Ferrara, JL, Holler, E, Stadler, M, Kolb, H-J, Zander, AR, Zürbig, P, Kellmann, M & Ganser, A 2007, 'Proteomic patterns predict acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation.', BLOOD, Jg. 109, Nr. 12, 12, S. 5511-5519. <http://www.ncbi.nlm.nih.gov/pubmed/17339419?dopt=Citation>

APA

Weissinger, E. M., Schiffer, E., Hertenstein, B., Ferrara, J. L., Holler, E., Stadler, M., Kolb, H-J., Zander, A. R., Zürbig, P., Kellmann, M., & Ganser, A. (2007). Proteomic patterns predict acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation. BLOOD, 109(12), 5511-5519. [12]. http://www.ncbi.nlm.nih.gov/pubmed/17339419?dopt=Citation

Vancouver

Weissinger EM, Schiffer E, Hertenstein B, Ferrara JL, Holler E, Stadler M et al. Proteomic patterns predict acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation. BLOOD. 2007;109(12):5511-5519. 12.

Bibtex

@article{f90e53d666c44e5786535b13bcde92ae,
title = "Proteomic patterns predict acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation.",
abstract = "Acute graft-versus-host disease (aGvHD) contributes significantly to morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Diagnosis of GvHD is mainly based on clinical features and tissue biopsies. A noninvasive, unbiased laboratory test for GvHD diagnosis does not exist. Here we describe the application of capillary electrophoresis coupled online with mass spectrometry (CE-MS) to 13 samples from 10 patients with aGvHD of grade II or more and 50 control samples from 23 patients without GvHD. About 170 GvHD-specific polypeptides were detected and a tentatively aGvHD-specific model consisting of 31 polypeptides was chosen, allowing correct classification of 13 of 13 (sensitivity 100.0% [95% confidence interval {CI} 75.1 to 100.0]) aGvHD samples and 49 of 50 (specificity 98.0% [95% CI 89.3 to 99.7]) control samples of the training set. The subsequent blinded evaluation of 599 samples enabled diagnosis of aGvHD greater than grade II, even prior to clinical diagnosis, with a sensitivity of 83.1% (95% CI 73.1 to 87.9) and a specificity of 75.6% (95% CI 71.6 to 79.4). Thus, high-resolution proteome analysis represents an unbiased laboratory-based screening method, enabling diagnosis, and possibly enabling preemptive therapy.",
author = "Weissinger, {Eva M} and Eric Schiffer and Bernd Hertenstein and Ferrara, {James L} and Ernst Holler and Michael Stadler and Hans-Jochem Kolb and Zander, {Axel R.} and Petra Z{\"u}rbig and Markus Kellmann and Arnold Ganser",
year = "2007",
language = "Deutsch",
volume = "109",
pages = "5511--5519",
journal = "BLOOD",
issn = "0006-4971",
publisher = "American Society of Hematology",
number = "12",

}

RIS

TY - JOUR

T1 - Proteomic patterns predict acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation.

AU - Weissinger, Eva M

AU - Schiffer, Eric

AU - Hertenstein, Bernd

AU - Ferrara, James L

AU - Holler, Ernst

AU - Stadler, Michael

AU - Kolb, Hans-Jochem

AU - Zander, Axel R.

AU - Zürbig, Petra

AU - Kellmann, Markus

AU - Ganser, Arnold

PY - 2007

Y1 - 2007

N2 - Acute graft-versus-host disease (aGvHD) contributes significantly to morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Diagnosis of GvHD is mainly based on clinical features and tissue biopsies. A noninvasive, unbiased laboratory test for GvHD diagnosis does not exist. Here we describe the application of capillary electrophoresis coupled online with mass spectrometry (CE-MS) to 13 samples from 10 patients with aGvHD of grade II or more and 50 control samples from 23 patients without GvHD. About 170 GvHD-specific polypeptides were detected and a tentatively aGvHD-specific model consisting of 31 polypeptides was chosen, allowing correct classification of 13 of 13 (sensitivity 100.0% [95% confidence interval {CI} 75.1 to 100.0]) aGvHD samples and 49 of 50 (specificity 98.0% [95% CI 89.3 to 99.7]) control samples of the training set. The subsequent blinded evaluation of 599 samples enabled diagnosis of aGvHD greater than grade II, even prior to clinical diagnosis, with a sensitivity of 83.1% (95% CI 73.1 to 87.9) and a specificity of 75.6% (95% CI 71.6 to 79.4). Thus, high-resolution proteome analysis represents an unbiased laboratory-based screening method, enabling diagnosis, and possibly enabling preemptive therapy.

AB - Acute graft-versus-host disease (aGvHD) contributes significantly to morbidity and mortality after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Diagnosis of GvHD is mainly based on clinical features and tissue biopsies. A noninvasive, unbiased laboratory test for GvHD diagnosis does not exist. Here we describe the application of capillary electrophoresis coupled online with mass spectrometry (CE-MS) to 13 samples from 10 patients with aGvHD of grade II or more and 50 control samples from 23 patients without GvHD. About 170 GvHD-specific polypeptides were detected and a tentatively aGvHD-specific model consisting of 31 polypeptides was chosen, allowing correct classification of 13 of 13 (sensitivity 100.0% [95% confidence interval {CI} 75.1 to 100.0]) aGvHD samples and 49 of 50 (specificity 98.0% [95% CI 89.3 to 99.7]) control samples of the training set. The subsequent blinded evaluation of 599 samples enabled diagnosis of aGvHD greater than grade II, even prior to clinical diagnosis, with a sensitivity of 83.1% (95% CI 73.1 to 87.9) and a specificity of 75.6% (95% CI 71.6 to 79.4). Thus, high-resolution proteome analysis represents an unbiased laboratory-based screening method, enabling diagnosis, and possibly enabling preemptive therapy.

M3 - SCORING: Zeitschriftenaufsatz

VL - 109

SP - 5511

EP - 5519

JO - BLOOD

JF - BLOOD

SN - 0006-4971

IS - 12

M1 - 12

ER -