Авторы

  • Kahramonjon Yuldashev
    Fergana Public Health Medical Institute., assistant.
  • Nosirjon Mahkamov
    Andijan State Medical Institute, DSc, Professor

DOI:

https://doi.org/10.71337/inlibrary.uz.mmms.135566

Аннотация

Nasal polyposis (NP) is a chronic inflammatory disease of the sinonasal mucosa, often associated with structural abnormalities such as post-traumatic nasal septum deviation. Persistent inflammation following trauma induces repeated immune activation, leading to polyp formation and remodeling of the mucosal architecture. The immune response, however, is strongly influenced by patient age, resulting in distinct patterns of immunohistochemical marker expression. Understanding these differences is crucial for clarifying disease pathogenesis and developing age-specific therapeutic approaches.


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MODELS AND METHODS IN MODERN SCIENCE

International scientific-online conference

133

DIFFERENCES IN IMMUNOHISTOCHEMICAL MARKER EXPRESSION

ACROSS AGE GROUPS IN POST-TRAUMATIC NASAL POLYPOSIS

Yuldashev Kahramonjon Shukurjon ugli

Fergana Public Health Medical Institute., assistant.

Mahkamov Nosirjon Juraevich

Andijan State Medical Institute, DSc, Professor

https://doi.org/10.5281/zenodo.17008023

Introduction

Nasal polyposis (NP) is a chronic inflammatory disease of the sinonasal

mucosa, often associated with structural abnormalities such as post-traumatic
nasal septum deviation. Persistent inflammation following trauma induces
repeated immune activation, leading to polyp formation and remodeling of the
mucosal architecture. The immune response, however, is strongly influenced by
patient age, resulting in distinct patterns of immunohistochemical marker
expression. Understanding these differences is crucial for clarifying disease
pathogenesis and developing age-specific therapeutic approaches.

Objective

To investigate age-related differences in the expression of

immunohistochemical markers (CD3, CD20, CD68, IFN-γ, IL-4, IL-5, IgE, and
TGF-β) in patients with post-traumatic nasal polyposis.

Materials and Methods

1. The study included

40 patients

aged 18–60 years diagnosed with post-

traumatic nasal polyposis.

2. Patients were divided into two age groups:

-

Group I: 18–35 years (20 patients)

-

Group II: 36–60 years (20 patients)

3. Polyp tissue samples were collected during endoscopic surgery.
4. Immunohistochemical staining was performed to assess the expression

of CD3, CD20, CD68, IFN-γ, IL-4, IL-5, IgE, and TGF-β.

5. Quantitative analysis was carried out using morphometric evaluation and

comparative statistics between the two groups.

Results
1. Younger patients (18–35 years):

- Higher infiltration of CD3+ T-lymphocytes and CD20+ B-lymphocytes was

detected.

- Expression of IL-4 and IL-5 was significantly increased, indicating a

dominant Th2 immune response.


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MODELS AND METHODS IN MODERN SCIENCE

International scientific-online conference

134

- Local IgE accumulation was frequently observed, accompanied by

eosinophil-rich infiltration.

- Clinically, these patients demonstrated recurrent disease episodes and a

more active inflammatory course.

2. Older patients (36–60 years):

- Predominant infiltration of CD68+ macrophages and increased fibroblast

activity were observed.

- Expression of IFN-γ was elevated, suggesting a dominant Th1 immune

response.

- TGF-β expression was markedly higher, consistent with fibrotic

remodeling processes.

- Clinically, patients demonstrated a more chronic, stable disease course,

with less frequent acute recurrences compared to younger patients.

Conclusion

Post-traumatic nasal polyposis demonstrates distinct age-related

differences in immunohistochemical marker expression:

1. Younger patients exhibit a Th2-skewed immune profile with increased

eosinophilic infiltration and IgE expression, correlating with an active and
recurrent clinical course.

2. Older patients demonstrate a Th1-predominant immune profile with

macrophage infiltration and fibrotic remodeling mediated by TGF-β, correlating
with a more stable but chronic disease progression.

These

findings

underscore

the

importance

of

age-specific

immunopathological evaluation in guiding personalized treatment strategies for
post-traumatic nasal polyposis.

References:

1. Fokkens WJ, Lund VJ, Hopkins C, et al. European Position Paper on
Rhinosinusitis and Nasal Polyps 2020. Rhinology. 2020;58(S29):1–464.
2. Schleimer RP. Immunopathogenesis of chronic rhinosinusitis and nasal
polyposis. Annu Rev Pathol. 2017;12:331–357.
3. Van Bruaene N, Perez-Novo CA, Basinski TM, et al. T-cell regulation in chronic
paranasal sinus disease. J Allergy Clin Immunol. 2008;121(6):1435–1441.
4. Akdis CA, Bachert C, Cingi C, et al. Endotypes and phenotypes of chronic
rhinosinusitis: A PRACTALL document. Allergy. 2013;68(6):731–751.
5. Bachert C, Zhang N, Holtappels G, De Lobel L, van Cauwenberge P. Nasal
polyposis: Molecular and cellular mechanisms. Allergy. 2007;62(4):331–341.
6. Soyka MB, Wawrzyniak P, Eiwegger T, et al. Defective epithelial barrier in
chronic rhinosinusitis. J Allergy Clin Immunol. 2012;130(5):1087–1096.

Библиографические ссылки

Fokkens WJ, Lund VJ, Hopkins C, et al. European Position Paper on Rhinosinusitis and Nasal Polyps 2020. Rhinology. 2020;58(S29):1–464.

Schleimer RP. Immunopathogenesis of chronic rhinosinusitis and nasal polyposis. Annu Rev Pathol. 2017;12:331–357.

Van Bruaene N, Perez-Novo CA, Basinski TM, et al. T-cell regulation in chronic paranasal sinus disease. J Allergy Clin Immunol. 2008;121(6):1435–1441.

Akdis CA, Bachert C, Cingi C, et al. Endotypes and phenotypes of chronic rhinosinusitis: A PRACTALL document. Allergy. 2013;68(6):731–751.

Bachert C, Zhang N, Holtappels G, De Lobel L, van Cauwenberge P. Nasal polyposis: Molecular and cellular mechanisms. Allergy. 2007;62(4):331–341.

Soyka MB, Wawrzyniak P, Eiwegger T, et al. Defective epithelial barrier in chronic rhinosinusitis. J Allergy Clin Immunol. 2012;130(5):1087–1096.