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CD177 EXPRESSION IN PERIPHERAL BLOOD NEUTROPHILS IN HEALTH AND DISEASE STATES
Author(s): ,
Aya Arafat
Affiliations:
Clinical and chemical pathology,Cairo university,Cairo,Egypt
,
Samia Rizk
Affiliations:
Clinical and chemical pathology,Cairo university,Cairo,Egypt
,
Rania Samy
Affiliations:
Clinical and chemical pathology,Cairo university,Cairo,Egypt
,
Noha Al-Husseiny
Affiliations:
Internal medicine,Cairo university,Cairo,Egypt
Rabab El-Hawary
Affiliations:
Clinical and chemical pathology,Cairo university,Cairo,Egypt
(Abstract release date: 05/18/17) EHA Library. Arafat A. 05/18/17; 182743; PB2029
Aya Arafat
Aya Arafat
Contributions
Abstract

Abstract: PB2029

Type: Publication Only

Background
Objective and specific assays are required in the identification of both chronic myeloproliferative disorders and myelodysplastic syndromes.

Aims

Exploration of the possibility of using the CD177 expression in the peripheral blood neutrophils for the diagnosis of either entity.

Methods
The 213 subjects were organized into 4 main groups; benign neutrophil leukocytosis group, secondary erythrocytosis group and clonal myeloid neoplasms group together with a haematologically normal group as controls. All cases were subjected to clinical assessment as well as the flow cytometry determination of the percentage (%) and mean fluorescent intensity (MFI) of peripheral blood neutrophils expressing CD177.

Results

Skewed high peripheral blood neutrophil CD177 MFI was significantly associated with Philadelphia-negative cMPDs patients (2.9-37.4; median 14.1) compared to controls (0.8-20.5; median 8.8). The MDS patients did not show a significant difference in either CD177 % or MFI compared to the controls. Polycythemia Vera (PV) patients had similar results of CD177 expression (% and MFI) compared to Essential Thrombocytosis (ET) patients. However, they had higher CD177 MFI levels compared to the secondary erythrocytosis patients and controls (4.8-37.4; median 16.5, 1.58-25.7; median 5.81, 0.85-20.5; median 8.8 respectively). CD177 MFI showed statistically significant higher values in ET patients compared to the haematologically normal control group (2.9-34.5; median 13.4 versus 0.85-20.5; median 8.8 respectively). No correlation between CD177 expression and JAK2 V617F allele burden could be detected in either PV or ET patients. With a 20 p.d.u cutoff, the specificity of neutrophil CD177 MFI in Philadelphia-negative cMPDs patients’ diagnosis and differentiation of PV from secondary erythrocytosis was 93% and 85% respectively. The CD177 % had a low accuracy of in the diagnosis of MDS patients. The CD177 patterns observed were one positive peak and bimodal pattern (Figure1).
Figure 1: Patterns of peripheral blood neutrophil CD177+ve cells expression observed in flow cytometry. A) Bimodal pattern. B, C, D, E) CD177 single positive peak varieties.

Conclusion

The CD177 expression is highly associated with Philadelphia-negative cMPDs. It could reliably represent a useful potential marker in detecting those disorders and differentiating them from reactive cases.

Session topic: 15. Myeloproliferative neoplasms - Biology

Keyword(s): Neutrophil, Myeloproliferative disorder, Myelodysplasia

Abstract: PB2029

Type: Publication Only

Background
Objective and specific assays are required in the identification of both chronic myeloproliferative disorders and myelodysplastic syndromes.

Aims

Exploration of the possibility of using the CD177 expression in the peripheral blood neutrophils for the diagnosis of either entity.

Methods
The 213 subjects were organized into 4 main groups; benign neutrophil leukocytosis group, secondary erythrocytosis group and clonal myeloid neoplasms group together with a haematologically normal group as controls. All cases were subjected to clinical assessment as well as the flow cytometry determination of the percentage (%) and mean fluorescent intensity (MFI) of peripheral blood neutrophils expressing CD177.

Results

Skewed high peripheral blood neutrophil CD177 MFI was significantly associated with Philadelphia-negative cMPDs patients (2.9-37.4; median 14.1) compared to controls (0.8-20.5; median 8.8). The MDS patients did not show a significant difference in either CD177 % or MFI compared to the controls. Polycythemia Vera (PV) patients had similar results of CD177 expression (% and MFI) compared to Essential Thrombocytosis (ET) patients. However, they had higher CD177 MFI levels compared to the secondary erythrocytosis patients and controls (4.8-37.4; median 16.5, 1.58-25.7; median 5.81, 0.85-20.5; median 8.8 respectively). CD177 MFI showed statistically significant higher values in ET patients compared to the haematologically normal control group (2.9-34.5; median 13.4 versus 0.85-20.5; median 8.8 respectively). No correlation between CD177 expression and JAK2 V617F allele burden could be detected in either PV or ET patients. With a 20 p.d.u cutoff, the specificity of neutrophil CD177 MFI in Philadelphia-negative cMPDs patients’ diagnosis and differentiation of PV from secondary erythrocytosis was 93% and 85% respectively. The CD177 % had a low accuracy of in the diagnosis of MDS patients. The CD177 patterns observed were one positive peak and bimodal pattern (Figure1).
Figure 1: Patterns of peripheral blood neutrophil CD177+ve cells expression observed in flow cytometry. A) Bimodal pattern. B, C, D, E) CD177 single positive peak varieties.

Conclusion

The CD177 expression is highly associated with Philadelphia-negative cMPDs. It could reliably represent a useful potential marker in detecting those disorders and differentiating them from reactive cases.

Session topic: 15. Myeloproliferative neoplasms - Biology

Keyword(s): Neutrophil, Myeloproliferative disorder, Myelodysplasia

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