Short Communication - Journal of Clinical Pathology and Laboratory Medicine (2023) Volume 5, Issue 6
Immunohistochemistry: Cellular precision medicine
Iula Trapani*
Department of Infectiology, Emory University, United States
- *Corresponding Author:
- Iula Trapani
Department of Infectiology, Emory University, United States
Emory University
United States
E-mail:paniula.23@edu.in
Received:27-Nov-2023, Manuscript No. AACPLM-23-121801; Editor assigned: 30-Nov-2023, PreQC No. AACPLM-23-121801(PQ); Reviewed:14-Dec-2023, QC No. AACPLM-23-121801; Revised:19-Dec -2023, Manuscript No. AACPLM-23-121801(R); Published:26-Dec-2023, DOI:10.35841/ aacplm-5.6.182
Citation: Iula T. Immunohistochemistry: Cellular precision medicine. J Clin Path Lab Med. 2023;5(6):182
Introduction
In the intricate landscape of modern medicine, the field of immunohistochemistry (IHC) stands as a powerful tool, offering a window into the cellular composition and molecular landscape of tissues. This indispensable technique, merging the principles of immunology and histology, allows for the precise identification and characterization of specific proteins within tissues, revolutionizing diagnostics, prognostics, and the development of targeted therapies[1].
At its core, immunohistochemistry utilizes the specific binding properties of antibodies to target and visualize proteins of interest within tissue sections. This technique enables the identification of cellular components, subcellular structures, and molecular markers, elucidating intricate details of tissue architecture and pathological alterations[2].
One of the primary applications of immunohistochemistry lies in disease diagnosis and classification. By targeting specific proteins associated with various diseases, such as tumor markers, infectious agents, or tissue-specific antigens, IHC aids pathologists in differentiating between different types of cancer, identifying infectious organisms, and characterizing tissue abnormalities[3].
Moreover, immunohistochemistry plays a pivotal role in predicting patient outcomes and guiding treatment decisions. It enables the assessment of biomarkers associated with prognosis and treatment response, facilitating personalized medicine[4].
In the realm of research, immunohistochemistry serves as an indispensable tool for elucidating disease mechanisms and exploring novel therapeutic targets. It allows scientists to delve into the intricate interplay of proteins, signalling pathways, and cellular interactions within tissues, paving the way for the development of innovative treatments[5].
The technique's versatility extends beyond oncology, finding applications in various fields including neurology, immunology, dermatology, and infectious diseases. In neurology, IHC aids in the characterization of neurodegenerative diseases, while in dermatology, it helps identify specific markers associated with skin conditions. Furthermore, IHC contributes to understanding immune responses in infectious diseases, aiding in the identification of pathogens within tissues[6,7].
However, challenges persist in the realm of immunohistochemistry, including standardization of protocols, interpretation variability, and the need for continuous advancements in antibody technology and image analysis techniques[8].
As we celebrate the strides made in immunohistochemistry, it's evident that this technique remains pivotal in unlocking the mysteries hidden within tissues. Its role in disease diagnosis, prognosis, treatment guidance, and research underscores its significance in advancing precision medicine[9].
In conclusion, immunohistochemistry stands as a beacon in deciphering cellular intricacies, offering insights crucial for understanding diseases and tailoring therapies. As technology evolves and our understanding deepens, the future promises further advancements in immunohistochemistry, solidifying its position as an indispensable ally in the quest for improved patient care and medical breakthroughs[10].
References
- Adams JC. Biotin amplification of biotin and horseradish peroxidase signals in histochemical stains. J Histochem Cytochem. 1992;40(10):1457-63.
- Arnold MM, Srivastava S, Fredenburgh J, et al. Effects of fixation and tissue processing on immunohistochemical demonstration of specific antigens. Biotech Histochem. 1996;71(5):224-30.
- Banerjee DI, Pettit SA. Endogenous avidin-binding activity in human lymphoid tissue. J Clin Pathol. 1984;37(2):223-5.
- Battifora H. Quality assurance issues in immunohistochemistry. J Histotechnol. 1999;22(3):169-75.
- Battifora H, Kopinski M. The influence of protease digestion and duration of fixation on the immunostaining of keratins. A comparison of formalin and ethanol fixation. J Histochem Cytochem. 1986;34(8):1095-100.
- Bendayan M. Possibilities of false immunocytochemical results generated by the use of monoclonal antibodies: the example of the anti-proinsulin antibody. J Histochem Cytochem. 1995;43(9):881-6.
- Boenisch T. Diluent buffer ions and pH: their influence on the performance of monoclonal antibodies in immunohistochemistry. Appl Immunohistochem Mol Morphol. 1999;7(4):300.
- Boenisch T. Formalin-fixed and heat-retrieved tissue antigens: a comparison of their immunoreactivity in experimental antibody diluents. Appl Immunohistochem Mol Morphol. 2001;9(2):176-9.
- Bork P, Doolittle RF. Proposed acquisition of an animal protein domain by bacteria. Proc Natl Acad Sci. 1992;89(19):8990-4.
- Bussolati GI, Gugliotta PA. Nonspecific staining of mast cells by avidin-biotin-peroxidase complexes (ABC). J Histochem Cytochem. 1983;31(12):1419-21.
Indexed at, Google Scholar, Cross Ref
Indexed at, Google Scholar, Cross Ref
Indexed at, Google Scholar, Cross Ref
Indexed at, Google Scholar, Cross Ref
Indexed at, Google Scholar, Cross Ref
Indexed at, Google Scholar, Cross Ref
Indexed at, Google Scholar, Cross Ref
Indexed at, Google Scholar, Cross Ref
Indexed at, Google Scholar, Cross Ref