Caspase: A family of cysteine proteases that cleave after an aspartate residue. The term caspase incorporates these elements (cysteine, aspartate, protease), which play important roles in the chain of reactions that leads to apoptosis.
Anaphylatoxins: The complement split products C3a and C5a, which mediate degranulation of mast cells and basophils, resulting in release of mediators that induce contraction of smooth muscle and increased vascular permeability.
Iccosomes: Immune-complex-coated cell fragments often found coating the spines of follicular dendritic cells.
Monday, April 21, 2014
Thursday, April 17, 2014
Dictionary #4
Dark Zone: A portion of the germinal center that is the site of rapid cell division by forms of B cells called centroblasts.
Superantigens: Any substance that binds to the V-beta domain of the T-cell receptor and residues in the chain of class II MHC molecules. It induces activation of all T cells that express T-cell receptors with a particular V-beta domain. It functions as a potent T-cell mitogen and may cause food poisoning and other disorders.
Tapasin: TAP-associated protein. Found in the ER that brings the TAP transporter into proximity with the class I MHC molecule, allowing it to associate with antigenic peptide.
Superantigens: Any substance that binds to the V-beta domain of the T-cell receptor and residues in the chain of class II MHC molecules. It induces activation of all T cells that express T-cell receptors with a particular V-beta domain. It functions as a potent T-cell mitogen and may cause food poisoning and other disorders.
Tapasin: TAP-associated protein. Found in the ER that brings the TAP transporter into proximity with the class I MHC molecule, allowing it to associate with antigenic peptide.
Wednesday, April 9, 2014
Reflections #3
As we near the end of the school
year, I cannot believe how fast time passes by. It seems like it was just
yesterday when we started learning about Immunology. Before I took this class I
knew nothing about the immune system except that it protects our body from
sicknesses and that it involves white blood cells. Now I feel like an expert
(although I’m not). We learned and covered many topics over the course of the
semester such the innate immune system, the adaptive immune system, the characteristics and
functions of different types of white blood cells, antigen processing and
presentation, the organs of the immune system, the different classes and
functions of different antibodies, the structure of B and T cells, MHC, and
cytokines. Although it may seem a lot of material, there is so much more to
learn.
The knowledge that I gained from
this semester will form the foundation that I will need as I continue my
education into the Medical Laboratory Science program. I saw in my course
outline that some of the courses are based off Immunology such as
Immunohematology, Clinical Immunology and Molecular Diagnostics, and Clinical
Bacteriology. The
labs this semester was beneficial, especially the ELISA test lab, ABO blood
typing, and counting the different white blood cells because I had a small
glimpse of what medical laboratory scientists work with. If I found the
labs this semester fun, I cannot wait what my clinical year in medical
laboratory science has in store.
Friday, April 4, 2014
Investigations #3
Today in my Animal Physiology
class, I saw a picture of a person who had severe swelling of the feet. I was
shocked and intrigued at the same time, so I decided to do a little
investigation about a disease called elephantiasis. The disease also known as
lymphatic filariasis affects over 90 million people in the world, particularly
in the tropical and subtropical parts of the world. The disease is
characterized by edema with thickening tissues, especially in the legs, arms, and
the genitals.
The disease is transmitted by
Filarial worms that are ingested by arthropod vectors like mosquitoes, which
would then be transmitted to humans when they bite humans for blood. The
infection causes a great inflammatory immune response, which results in the development
of symptomatic lymphatic obstruction. The larvae of the Filarial worms migrate towards the lymphatic vessels where they would develop to adult worms. The full mechanism of this disease is
still not completely understood. However, it is known that there is an increase
in the levels of IgE and IgG4. In addition, people who are infected with this
disease have been found to have an impaired lymphocyte proliferation response
to the Filarial worms and have defects in the antigen-presenting cells function.
Studies have found that genetic polymorphism in the parasite and/or host may
influence the susceptibility to the infection.
Unfortunately, there is currently
no vaccine that is available for this disease. People who live in areas that
are at risk of the disease would be given two drugs annually – albendazole with
invermectin or with diethylcarbamazine citrate – to prevent the spread of the
infection. Although the disease is rarely fatal, it is important to treat the
disease early to prevent severe disability.
Works Cited
King,
C.L. Transmission intensity and human immune responses to lymphatic filariasis.
Parasite Immunology 2001; 23.
Wayangankar, S. [Internet] Filariasis; 2013 [Cited 2014 April 4]. Available from: http://emedicine.medscape.com/article/217776-overview#a0156
World
Health Organization [Internet]. WHO; 2014 [Cited 2014 April 4]. Available from: http://www.who.int/mediacentre/factsheets/fs102/en/
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