Why blood of bird flu survivors is a lifesaver [Discussion]
Those of you who have read my posts before are probably aware I am not expecting there to be useful quantities of vaccine during the first wave or waves of a pandemic and that I expect any pandemic form of the virus to develop Tamiflu resistance in short order – I will not reiterate my reasoning here.
Anything that looks like it has the potential to mitigate the effects of a sever pandemic and be scaleable, at reasonable cost, tends to catch my attention – does this meet those criteria?
How specific are the Anti bodies? Does it work like vaccine and to the same extent? i.e. if the flu which caused the creation of the anti bodies was 97% homologous with the pandemic strain would the fall off in protection be akin to the fall off from a 97% homologous vaccine? Is it more – or less - strain specific?
“In the event of a flu pandemic, it would be necessary to wait until a first wave of patients had recovered” – If Jones Gitting donated a litre of his blood how could this be scaled up? What production facilities are required? Do we need humans or can we use cattle (BSE tested) or cell culture?
From my meagre (and quite possibly erroneous) understanding of the immune system, undifferentiated B Cells on contact with an antigenic site on the HA or NA of the flu’s surface convert to Plasma Cells producing antibodies specific to that antigenic site. Post infection, the number of these specific Plasma Cells are reduced but a few remain for quick response in the case of re-infection by a virus with the same surface antigen. If this is basically correct (if it is not please edit or post a correction so I am not misleading anyone) then how does the immune system react to the introduction of an antibody not an antigen (i.e. the key not the lock)? Is there an adjuvant analogue?
What is the difference in the level of protection offered by this form of immunisation compared to traditional vaccines?
If immune overreaction (cytokine storm) turns out to be a major cause of clinical severity & death does this form of immune system prepping differ form that of traditional vaccines?
The article talks about this system being used for hepatitis A, chicken pox and measles but not flu "The approach has not yet been used against flu in humans, largely because existing vaccines and antivirals are more effective and less risky." Why?
As you can see I am quite good at generating questions, just not so good on the answers. Help please.
Those of you who have read my posts before are probably aware I am not expecting there to be useful quantities of vaccine during the first wave or waves of a pandemic and that I expect any pandemic form of the virus to develop Tamiflu resistance in short order – I will not reiterate my reasoning here.
Anything that looks like it has the potential to mitigate the effects of a sever pandemic and be scaleable, at reasonable cost, tends to catch my attention – does this meet those criteria?
• Immunoglobulins are antibodies produced by the immune system to fight germs
• When patients recover from a disease their blood contains antibodies against it, giving them an immunity
• These antibodies can be recovered by drawing blood from a patient and “fractionating” it to isolate immunoglobulins
• Immunoglobulins can be injected into another patient to boost his or her immune system’s response
• Immunoglobulin treatments are used against diseases including hepatitis A, chicken pox and measles
• In the event of a flu pandemic, it would be necessary to wait until a first wave of patients had recovered from infection with the dangerous strain before isolating the relevant antibodies
• It should take only a few weeks to make immunoglobulin treatments
• Immunoglobulins would not replace the need for vaccines and antiviral drugs like Tamiflu. It would be valuable as an alternative treatment, however, if the virus developed a resistance to Tamiflu
• When patients recover from a disease their blood contains antibodies against it, giving them an immunity
• These antibodies can be recovered by drawing blood from a patient and “fractionating” it to isolate immunoglobulins
• Immunoglobulins can be injected into another patient to boost his or her immune system’s response
• Immunoglobulin treatments are used against diseases including hepatitis A, chicken pox and measles
• In the event of a flu pandemic, it would be necessary to wait until a first wave of patients had recovered from infection with the dangerous strain before isolating the relevant antibodies
• It should take only a few weeks to make immunoglobulin treatments
• Immunoglobulins would not replace the need for vaccines and antiviral drugs like Tamiflu. It would be valuable as an alternative treatment, however, if the virus developed a resistance to Tamiflu
“In the event of a flu pandemic, it would be necessary to wait until a first wave of patients had recovered” – If Jones Gitting donated a litre of his blood how could this be scaled up? What production facilities are required? Do we need humans or can we use cattle (BSE tested) or cell culture?
From my meagre (and quite possibly erroneous) understanding of the immune system, undifferentiated B Cells on contact with an antigenic site on the HA or NA of the flu’s surface convert to Plasma Cells producing antibodies specific to that antigenic site. Post infection, the number of these specific Plasma Cells are reduced but a few remain for quick response in the case of re-infection by a virus with the same surface antigen. If this is basically correct (if it is not please edit or post a correction so I am not misleading anyone) then how does the immune system react to the introduction of an antibody not an antigen (i.e. the key not the lock)? Is there an adjuvant analogue?
What is the difference in the level of protection offered by this form of immunisation compared to traditional vaccines?
If immune overreaction (cytokine storm) turns out to be a major cause of clinical severity & death does this form of immune system prepping differ form that of traditional vaccines?
The article talks about this system being used for hepatitis A, chicken pox and measles but not flu "The approach has not yet been used against flu in humans, largely because existing vaccines and antivirals are more effective and less risky." Why?
As you can see I am quite good at generating questions, just not so good on the answers. Help please.
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