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Immunoglobulin-like Cell Adhesion Molecules01:31

Immunoglobulin-like Cell Adhesion Molecules

Immunoglobulin-like cell adhesion molecules or Ig-CAMs are a versatile group of cell surface glycoproteins belonging to the immunoglobulin protein superfamily. Ig-CAMs possess the characteristic immunoglobulin protein domains and other domains such as the fibronectin type III domain. The Ig domains are glycosylated to varying degrees in different Ig-CAMs.
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
Disorders of Leukocytes01:27

Disorders of Leukocytes

Leukocyte disorders can lead to either leukopenia, characterized by an abnormally low leukocyte count, or leukocytosis, marked by a very high leukocyte number.
Leukopenia may result from bone marrow disorders, autoimmune diseases, and infectious diseases. For example, conditions such as multiple myeloma and aplastic anemia can impair the bone marrow's ability to produce adequate leukocytes. Similarly, autoimmune diseases like lupus and viral infections such as HIV can prompt the immune system...
Special Features of Adaptive Immunity01:20

Special Features of Adaptive Immunity

The adaptive immune system, a crucial component of the overall immune response, offers a highly specialized defense against pathogens. It involves specific cell types and features, enabling it to combat infections effectively and efficiently.
The primary cell types involved in adaptive immunity are T cells and B cells. Each type has a unique role in defending the body against pathogens. T cells are responsible for cell-mediated immunity. They identify and eliminate infected cells directly,...
Immunodeficiency Diseases01:25

Immunodeficiency Diseases

Immunodeficiency disorders are conditions in which the immune system's ability to fight infectious disease and cancer is compromised or entirely absent. The immune system comprises a complex network of cells, tissues, and organs that work together to protect the body from potentially harmful invaders. When this system is deficient or not functioning properly, it leaves the body susceptible to infections, diseases, or other complications.
There are three main causes of immunodeficiency disorders...
Atypical Pneumonia01:14

Atypical Pneumonia

Atypical pneumonia, often caused by Mycoplasma pneumoniae, is a form of pulmonary infection that differs from the classical presentation of bacterial pneumonia in both its cause and clinical symptoms. Mycoplasma pneumoniae is a pleomorphic bacterium notable for its lack of a rigid cell wall. This structural characteristic imparts resistance to beta-lactam antibiotics and significantly influences the bacterium’s behavior within the human host.Other pathogens responsible for the disease include...
Cryptococcal Meningitis01:27

Cryptococcal Meningitis

Cryptococcal meningitis is a life-threatening opportunistic infection predominantly associated with HIV/AIDS, accounting for over 100,000 deaths annually worldwide. However, it also affects individuals with other forms of immunosuppression, including those undergoing immunosuppressive therapy, organ transplant recipients, patients with innate immunodeficiencies, and individuals with hematological disorders. The infection is caused mainly by Cryptococcus neoformans and Cryptococcus gattii,...

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Related Experiment Video

Updated: Jul 23, 2026

Characterization of Immune Cell-derived Extracellular Vesicles and Studying Functional Impact on Cell Environment
10:09

Characterization of Immune Cell-derived Extracellular Vesicles and Studying Functional Impact on Cell Environment

Published on: June 2, 2020

Vesiculobullous diseases with prominent immunologic features.

E E Boh, L E Millikan

    JAMA
    |November 25, 1992
    PubMed
    Summary

    Differentiating bullous skin diseases can be challenging. Diagnosis often requires skin biopsy and immunofluorescent studies to identify specific immunoreactants involved in pathogenesis.

    Area of Science:

    • Dermatology
    • Immunology
    • Pathology

    Background:

    • Bullous skin diseases encompass a diverse group of conditions.
    • Clinical presentation and age of onset offer initial diagnostic clues.
    • Accurate differentiation is crucial for effective patient management.

    Purpose of the Study:

    • To highlight the diagnostic challenges in differentiating bullous skin diseases.
    • To emphasize the role of specialized immunofluorescence techniques in diagnosis.
    • To explore the pathogenetic mechanisms involving the dermoepidermal basement membrane zone.

    Main Methods:

    • Clinical evaluation and patient history.
    • Skin biopsy for histopathological examination.
    • Direct immunofluorescence (DIF) and indirect immunofluorescence (IIF) studies, including split-skin variations.

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    Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis
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    Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis

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    Published on: June 2, 2020

    Isolating Central Nervous System Tissues and Associated Meninges for the Downstream Analysis of Immune cells
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    Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis
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    Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis

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    Main Results:

    • Clinical features alone are often insufficient for definitive diagnosis.
    • Immunofluorescence studies are essential for identifying specific disease-related immunoreactants.
    • These studies aid in distinguishing between various autoimmune blistering disorders.

    Conclusions:

    • Accurate diagnosis of bullous dermatoses relies on a combination of clinical and laboratory findings.
    • Immunofluorescence studies are indispensable tools for elucidating disease mechanisms.
    • Further research into dermoepidermal basement membrane zone immunoreactants may reveal novel therapeutic targets.