Spleen neoangiogenesis in patients with myelofibrosis with myeloid metaplasia

被引:44
|
作者
Barosi, G
Vittorio, R
Margherita, MS
Luca, VG
Alessandro, P
Vittorio, N
Isabella, R
Rita, C
Monia, M
Mario, B
Is, MNAEH
机构
[1] IRCCS, Policlin San Matteo, Lab Informat Med, I-27100 Pavia, Italy
[2] IRCCS, Policlin San Matteo, Transplant Res Area, I-27100 Pavia, Italy
[3] IRCCS, Policlin San Matteo, Biotechnol Lab, I-27100 Pavia, Italy
[4] IRCCS, Policlin San Matteo, Clin Immunol & Immunohematol & Transfus Serv, I-27100 Pavia, Italy
[5] IRCCS, Policlin San Matteo, Unit Internal Med & Med Oncol, I-27100 Pavia, Italy
[6] IRCCS, Policlin San Matteo, Inst Pathol, I-27100 Pavia, Italy
[7] IRCCS, Policlin San Matteo, Unit Internal Med 3, I-27100 Pavia, Italy
[8] Osped Vangelico Valdese, Hematol Unit, Turin, Italy
关键词
myelofibrosis; myeloid metaplasia; angiogenesis; CD34(+) cells; spleen angiogenesis;
D O I
10.1111/j.1365-2141.2004.04829.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neoangiogenesis is an integral component of bone marrow myeloproliferation in patients with myelofibrosis with myeloid metaplasia (MMM). As extramedullary haematopoiesis is a constitutive feature of MMM, we studied spleen neoangiogenesis by a computerized image analysis in MMM patients. Compared with five normal subjects, spleen CD34-staining capillary vascular density (CVD) was 2.1-3.03 times higher than the upper range of normal in six of the 15 (40%) MMM patients. CD8-staining sinusoidal vascular density (SVD) was constantly normal or lesser than normal and was inversely correlated with CVD (R=-0.53; P=0.04). In MMM patients who did not receive cytoreductive or radiation therapy in the month before splenectomy (n=9), the CVD was a significant determinant of spleen size (R=0.88; P=0.04). In MMM patients, the number of spleen CD34(+) haematopoietic stem cells was increased from 1.2 to 98 times the upper limit of normal, and predicted the expansion of CVD (R=0.57; P=0.03). A population of cells expressing the CD34(+)/CD133(+)/VEGFR-2(+) angiopoietic phenotype was present in the blood and spleen of five of seven patients. These results document that neoangiogenesis is an integral component of spleen re-localization of haematopoietic stem cells and suggest a cellular mechanism for spleen neoangiogenesis.
引用
收藏
页码:618 / 625
页数:8
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