Being drug addiction, Human antibody bolsters cancer | OneDayTop

Being drug addiction, Human antibody bolsters cancer

drug and alcohol dependence

As effective, the cancer drug rituximab does not work for everyone. Anyway, a new study says that adding a specific human antibody to the medication might restore its cancer-killing capabilities. Rituximab, which is sometimes sold under the brand name Rituxan, is used to treat certain autoimmune diseases and some types of cancer. Rituximab is not a chemotherapy drug. But rather a monoclonal antibody therapy that can be used either alone or alongside chemotherapy. This type of intervention uses antibodies. It’s bind to specific cells or proteins, thereby stimulating the patient’s immune system to attack them. Specifically, rituximab is an antibody against a protein called CD20, which occurs most commonly on the surface of immune B cells. Rituximab is useful in treating non-Hodgkin lymphoma and chronic lymphocytic leukemia; in these conditions, the cancer primarily affects the immune cells. Rtuximab is thought to work by using a number of mechanisms. For example, once the drug has bound to CD20, it forms a cap on one side of the cell, which draws proteins over to that side. When natural killer cells bind to the cap, they are more successful at triggering cell death, or apoptosis. In short time, rituximab helps the immune system to target and kill cancer cells more effectively. Drugs and alcohol dependence destroy the cancer antibody.

drug destroy the antibody


Researchers can design antibody treatment for cancer.  When rituximab was approved for medical use in 1997, it was well received. Some researchers have referred to it as the “most substantial advancement in the treatment of B cell malignancies, since the advent of combination chemotherapy.”  A group of researchers from the Duke Cancer Institute in Durham, NC, recently investigated this mechanism in more detail. They wanted to understand whether or not they could influence this counterproductive protective mechanism to improve the effectiveness of rituximab for more people. The team was led by senior author Dr. Edward F. P.  In earlier studies, Dr. Patz and his colleagues identified some patients who had antibodies to CFH, and who therefore had a natural ability to fight cancer. By producing this antibody, they were able to shut off CFH, effectively removing the cancer cell’s security system and leaving it open to the immune system or drugs such as rituximab.


In the most recent set of experiments, Dr. Patz set out to understand whether the antibody to CFH could make rituximab effective in patients who were naturally resistant to it. To begin, the researchers tested the leukemic cells of 11 patients in order to ascertain whether or not they were resistant to rituximab. Ten out of the 11 participants’ tumor cells were unresponsive to the drug. When the researchers added CFH antibody to rituximab, five of the 11 patients (45 percent) demonstrated a significant increase in the death of cancer cells. As Dr. Patz explains, “This is a combination approach, and it appears to strip away immune protection of cancer cells. Patients who had been rituximab resistant became rituximab sensitive. This future research will measure how it works on advanced solid tumors, including breast, colon, and lung cancers. A new study researchers say about the monoclonal antibodies and cancer. The more advanced our understanding of cancer becomes; the more complexities we find in the disease. This makes pushing for new treatments is an increasingly convoluted task.


As the conclusion we can say that drug can destroy the antibody. It is becoming increasingly clear that tumors use multiple mechanisms to evade the immune system and are often resistant to monotherapy. It’s a better understanding of resistance mechanisms will help optimize cancer therapy.

drug destroy the antibody


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