During pregnancy the antibodies and
antigens production levels are traced to be abnormal in women. Such changes can
affect the health of the mother and as well the new born along with
many complications during pregnancy. RBC Alloimmunization is also one such condition which occurs due to the formation of
antibodies to red blood cell antigens in the recipient from previous blood
transfusions or a pregnancy. Sometimes this condition is also traced when the
body is not exposed to foreign RBC antigens earlier before the transfusions.
The formation of antibodies in the
human body differs extensively depending on the patient’s disease, history of
transfusions, pregnancy and the rate of antigens production against the donors
of different geographical locations. In order to trace the level of RBC Alloimmunization keeping the record
of the antibody and antigen rates against the transfusions is important.
Normally, the rate of red cell antibodies is estimated to be 20% or more in
patients with transfusion dependent diseases like sickle cell
anemia and thalassemia etc.
Sickle-cell disease (SCD) is
an autosomal recessive genetic blood disorder with
over dominance, characterized by red blood cells that assume an
abnormal, rigid, sickle shape. Sickling decreases the cells flexibility
and results in a risk of various complications. The sickling occurs because of
a mutation in the hemoglobin gene during a transfusion.
However, Red blood cell transfusions have reduced despair and mortality for
patients with sickle cell disease. Transfusions can anyhow lead to RBC Alloimmunization.
Blood transfusion is an essential treatment for the
patients with sickle cell disease (SCD). However,
transfusions can lead to RBC
Alloimmunization with serious complications for the patient. These
antibodies produced in such conditions are often directed against antigens
expressed on RBC’s of white persons, donors of western countries. However, finding
such donors lacking those antigens can sometimes be difficult and identifying
and characterizing the antibodies can be a time consuming job causing
transfusion delays.
The most serious consequence of RBC Alloimmunization in SCD patients is
the risk of developing a delayed hemolytic transfusion reaction (DHTR), which
can be life taking. In many cases, the patient's hemoglobin level falls below
the pre transfusion level indicating that the patient own RBCs are lysed in
addition to hemolysis of the transfused RBCs. This condition is known as
hyperhemolysis. Additional transfusions may provoke the hemolysis and further
worsen the degree of anemia in the patients.
Not all patients develop all
antibodies after exposure to transfused RBCs. This fact pertains not only to
patients with SCD but also to other transfused recipients. RBC Alloimmunization cannot be entirely prevented except by
transfusions from an identical twin or by autologous transfusions. Preventing
RBC antibody formation is also not practical for most patients and, for man yit
causes no serious complications. But prevention of RBC Alloimmunization is important in women of child bearing age, and
for some patients at risk of serious haemolytic transfusion reactions. It is
currently unknown whether RBC
Alloimmunization rates differ depending on the presence or absence of
clinical complications of SCD.
In conclusion, challenges remain
for the diagnosis, prevention, and management of RBC Alloimmunization in SCD. Understanding the mechanisms and
associated risk factors will aid in developing strategies to prevent and
inhibit production of antibodies in transfused patients and to minimize its
life threatening complications resulting from transfusions. Also, Immuno
modulatory therapies, such as the use of immune cell depleting agents,
costimulatory blockade, and cytokine blockade, may be effective in suppressing RBC Alloimmunization in patients. Tracing
the conditions and taking timely precautions can help to recover from such
complications during the pregnancy.