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Detection of intracellular IgD using flow cytometry could be a novel and supplementary method to diagnose IgD
Wei Wang1, Chun-Xia Zhang1, Zhen-Ling Li1
1Hematology Department, China-Japan Friendship Hospital, Ying-Hua-Yuan East Street, No. 2, Beijing, 100029, China.
Insights
Detecting cytoplasmic immunoglobulin D (IgD) via flow cytometry is a sensitive and convenient supplemental method for diagnosing IgD multiple myeloma (MM). This technique aids in identifying specific subtypes of this plasma cell disorder.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Multiple myeloma (MM) is a plasma cell malignancy with diverse subtypes.
- Accurate diagnosis of IgD multiple myeloma (MM) is crucial for appropriate patient management.
- Current diagnostic methods may require supplemental approaches for specific MM subtypes.
Purpose of the Study:
- To evaluate the utility of detecting cytoplasmic immunoglobulin D (IgD) heavy chains using flow cytometry.
- To determine if this method can serve as a supplemental diagnostic tool for IgD MM.
- To assess the sensitivity and convenience of this flow cytometry-based approach.
Main Methods:
- Bone marrow samples from 35 MM patients were analyzed.
- Flow cytometry was employed to detect cytoplasmic immunoglobulin heavy chains (IgA, IgG, IgM, IgD).
- Samples included 5 IgD MM, 9 IgG MM, 10 IgA MM, 1 IgM MM, 9 light chain MM, and 1 non-secretory MM.
Main Results:
- All 5 IgD MM patients showed positive results for cytoplasmic IgD.
- The percentage of IgD-positive MM cells ranged from 0.4% to 12.9%.
- Other heavy chain subtypes (IgG, IgA, IgM) were detected in their respective MM subtypes, with no heavy chain detected in light chain or non-secretory MM.
Conclusions:
- Flow cytometry detection of cytoplasmic IgD is a practical and sensitive method.
- This technique can be used as a supplemental tool for diagnosing IgD multiple myeloma.
- The findings support the integration of this method into diagnostic workflows for MM.
Background:
We examined whether detecting the heavy chain of cytoplasmic immunoglobulin D (IgD) by flow cytometry could be used as a supplemental method to diagnose IgD multiple myeloma (MM).
Methods:
Bone marrow (BM) samples of thirty-five patients with MM were collected. Five of them were IgD MM, the rest of thirty were other subtypes of MM. Antibodies to four types of heavy chains of immunoglobulin (e.g., IgA, IgG, IgM, and IgD) were analyzed by flow cytometry in each patient's BM sample.
Results:
The five IgD MM patients were all positive for cytoplasmic IgD. The percentage of IgD positive MM cells among nucleated cells varied from 0.4 to 12.9%. Cytoplasmic IgG was positive in eight patients with IgG MM (n = 9); cytoplasmic IgA was positive in all patients with IgA MM (n = 10); cytoplasmic IgM was positive in one patient with IgM MM (n = 1). No heavy chain was detected in light chain MM (n = 9) and non-secretory subtype (n = 1).
Conclusions:
Detection of cytoplasmic IgD by flow cytometry is a convenient, sensitive and supplemental method to diagnose IgD MM.
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