Synonym |
CMV pp65 (495-503) |
Species |
Human Cytomegalovirus (HCMV) |
Protein Accession |
P06725 |
Purity |
> 95% |
Endotoxin Level |
< 1 EU/ug |
Biological Activity |
Not specified |
Expression System |
Insect cells |
Fusion Tag |
None |
Predicted Molecular Mass |
3.2 kDa |
Formulation |
Lyophilized |
Reconstitution |
Dissolve in PBS, pH 7.4 |
Storage & Stability |
Store at -20°C upon receipt, stable for up to 2 years |
FAQ
What is Human CMV pp65 (495-503) and what is its significance in research?
Human Cytomegalovirus
(CMV) is a prevalent virus that infects a significant portion of the adult population globally. One of
the key antigens of this virus is the pp65 protein, a matrix phosphoprotein that plays a crucial role in
the virus’s life cycle and immune evasion. The peptide sequence from 495 to 503 within this protein is
of particular interest due to its high immunogenic potential. It is known to be a target for CD8+ T-cell
responses, which are critical for controlling viral infections. Research involving pp65 (495-503) is
significant for understanding the immune response to CMV, which is important for developing vaccines and
therapies. By studying this specific peptide, researchers gain insights into how the immune system
recognizes and combats CMV, leading to advancements in medical interventions that can mitigate the
impact of CMV, especially in immunocompromised individuals, transplant patients, and
newborns.
What role does Human CMV pp65 (495-503) play in vaccine development?
Human CMV
pp65 (495-503) is a prominent target in vaccine development efforts due to its ability to elicit a
strong CD8+ T-cell immune response. This peptide epitope is recognized by the immune system's cytotoxic
T lymphocytes (CTLs), which are pivotal in controlling and clearing viral infections. In the context of
vaccine development, identifying and utilizing epitopes like pp65 (495-503) can lead to the design of
vaccines that effectively harness the body’s immune mechanisms to fight CMV. Researchers are exploring
ways to incorporate this peptide into vaccine formulations to ensure that the immune system is primed to
recognize and combat CMV upon exposure. This approach not only aids in preventing initial infections but
also in reducing viral loads and transmission rates in the population. In populations where CMV poses
severe risks, such as transplant recipients and immunocompromised individuals, a vaccine targeting this
specific immunodominant peptide could significantly enhance immune defense, decrease CMV-related
complications, and improve quality of life.
How can Human CMV pp65 (495-503) contribute to
immunotherapy advancements?
Human CMV pp65 (495-503) contributes to immunotherapy advancements by
serving as a potent epitope for triggering immune responses in therapeutic settings. In immunotherapy,
the objective is to bolster the immune system's ability to recognize and eliminate pathogens and cancer
cells. The pp65 (495-503) peptide is a well-defined cytotoxic T lymphocyte (CTL) epitope, meaning it is
recognized by CTLs which are instrumental in targeting and destroying infected or malignant cells.
Therapies based on this peptide aim to enhance or restore the immune responses in individuals whose
systems are compromised or suboptimal, such as patients with cancer or chronic viral infections. By
stimulating specific immune cells with this epitope, it's possible to tailor therapeutic interventions
to an individual's immunological profile, increasing efficiency and therapeutic outcomes. Such
personalized immunotherapies are on the cutting edge of biomedical research and hold the potential for
significant breakthroughs in managing diseases that evade conventional treatment strategies.
What
challenges exist in the research of Human CMV pp65 (495-503)?
Research on Human CMV pp65
(495-503) poses several challenges. First, CMV's ability to establish latency complicates the study of
immune responses to its epitopes; the virus can persist in individuals without active replication,
leading to sporadic immune activity that is difficult to measure and analyze consistently. Second, the
high variability in immune responses among different individuals presents a challenge; genetic factors
can affect how effectively a person's immune system recognizes and responds to the pp65 (495-503)
peptide. Third, CMV has developed numerous mechanisms to evade the host's immune system, and
understanding these requires complex and multifaceted research approaches. Fourth, creating accurate and
predictive in-vitro models that replicate the human immune response to CMV infection, including
responses to pp65 (495-503), remains an ongoing challenge in immunological research. These challenges
necessitate innovative methodologies and cross-disciplinary collaborations to unravel the complexities
of CMV pathology and host interactions.
How is the immune response to Human CMV pp65 (495-503)
assessed in research studies?
Assessing the immune response to Human CMV pp65 (495-503) in
research studies involves several methods that focus on detecting and measuring the activity of specific
T cells. Flow cytometry is commonly used to analyze the expression of surface markers and cytokines,
providing insights into T-cell activation and proliferation. Enzyme-linked immunospot (ELISPOT) assays
allow researchers to quantify the number of T cells secreting specific cytokines in response to the
peptide, giving a direct measure of the immune response's strength and specificity. Additionally,
intracellular cytokine staining can provide detailed data on cytokine production at the single-cell
level. These methodologies enable a comprehensive understanding of the cellular immune response to CMV
infection, aiding in the development of effective therapeutic and immunization strategies. Furthermore,
advances in genomic and proteomic technologies continue to enhance researchers' ability to dissect the
intricate responses of the immune system to this potent viral epitope.