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Updated: Mar 20, 2026

The Bovine Lung in Biomedical Research: Visually Guided Bronchoscopy, Intrabronchial Inoculation and In Vivo Sampling Techniques
Published on: July 3, 2014
Histological changes of conjunctiva-associated lymphoid tissue caused by pneumonia in Holstein young cows
Keigo Kosenda1, Yuki Ishiguro2, Yuto Sano2
1Laboratory of Farm Animal Pathophysiology, Division of Farm Animal Clinical Sciences, Department of Veterinary Medicine, Rakuno Gakuen University, Ebetsu, Japan.
Insights
Respiratory infections in cows can activate conjunctiva-associated lymphoid tissue (CALT). This immune tissue in the eye may enhance immune responses in the respiratory tract, offering potential for mucosal vaccination strategies.
Area of Science:
- Veterinary immunology
- Ocular immunology
- Mucosal immunology
Background:
- Conjunctiva-associated lymphoid tissue (CALT) is crucial for mucosal IgA production on ocular and respiratory surfaces.
- CALT is reportedly increased in cattle, suggesting its importance in bovine mucosal immunity.
- The conjunctiva's immunological link to the respiratory mucosa makes it a potential site for mucosal vaccination against respiratory infections in animals.
Purpose of the Study:
- To investigate whether chronic respiratory antigen stimulation, as seen in pneumonia, influences CALT morphology and function in cows.
- To compare CALT characteristics between pneumonia-infected and healthy cattle.
- To elucidate the immune interactions between the conjunctiva and respiratory mucosa in response to chronic antigen exposure.
Main Methods:
- Comparative morphological analysis of CALT in pneumonia-infected versus healthy cows.
- Assessment of CALT appearance rate, area, and immune cell distribution.
- Evaluation of epithelial discontinuity and IgA-positive cell counts in conjunctival tissues and lungs.
Main Results:
- No significant differences in CALT appearance rate, area, or immune cell distribution were observed between the groups.
- A higher percentage of discontinuous epithelial layers was found in the third eyelid lymphoid follicle of pneumonia-infected cows.
- Significantly increased numbers of IgA-positive cells were detected in the conjunctiva and lungs of cows with pneumonia.
Conclusions:
- Chronic respiratory antigen sensitization during pneumonia enhances antigen uptake and mucosal immune effector function in the bovine conjunctiva.
- Immune interactions between the conjunctiva and respiratory mucosa play a role in this response.
- Findings support the potential of the conjunctiva as a target for mucosal vaccination against bovine respiratory diseases.
Abstract:
Conjunctiva-associated lymphoid tissue (CALT) induces mucosal IgA production on the ocular surface and within the respiratory mucosa. Increased CALTs have been reported in cows. The conjunctiva represents a potential site for mucosal vaccinations against respiratory infections in animals due to the strong immunological relationship between the conjunctiva and the respiratory mucosae. However, it remains unclear whether respiratory antigen sensitization triggers CALT development and a subsequent conjunctival humoral immune response, particularly in cows. To clarify these mechanisms, we compared CALT morphology between pneumonia-infected cows with chronic respiratory antigen stimulation and healthy cows. There were no differences in the appearance rate, area, or immune cell distribution of CALT between the groups. The percentage of discontinuous epithelial layers covering the third eyelid lymphoid follicle was significantly higher in the cows with pneumonia than in the healthy cows. The numbers of IgA-positive cells in the eyelid and third eyelid conjunctival lamina propria were significantly higher in cows with pneumonia. Similarly, these animals exhibited numerous pulmonary IgA-positive cells. These results suggest that chronic respiratory antigen sensitization during pneumonia promotes antigen uptake and mucosal immune effector function in the bovine conjunctiva through immune interactions between the conjunctiva and respiratory mucosa.
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