「Meningococcus」の版間の差分
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52行目: | 52行目: | ||
*A,C,Y,W135 | *A,C,Y,W135 | ||
− | *B | + | ===issues of men B vaccine=== |
− | **B | + | *polysaccharide of B is relatively low immunogenic |
+ | **the reason | ||
+ | *polysaccharide of B has potential toxicity for infant brain | ||
+ | **PS of B shows interaction with fatal brain cells which suggests potential of causing neurological damage for young infants |
2021年6月1日 (火) 11:24時点における版
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目次
pathogen
- Neisseria meningitidis
- gram negative diplococci
- carriage in nasopharynx
- 12 identified capsular serogroups
- common pathogenic serogroup A, B, C, W, X, Y
- seasonal epidemics by group A, C
- meningitis belt
- sporadic cases by e.g. group B
- Latin America
- Norway
- New Zealand
- immunity generated by polysaccharide capsule except B
- may be the reason that herd immunity development relatively slow and sporadic outbreaks continue in above countries
epidemiology
- highest < 2 y/o and adolescent
- annual outbreak during dry season in meningitis belt
- dry winds make people's nose drier resulting in easy
- wide range difference of nasopharynx carriage between countries
- reason totally unknown
- NZ & 3%
- Nigeria boarding house 30-40%
transmission
- aerosol
- fomite
- adolescent activity
clinical picture
- fever
- distinctive petechiae anywhere in whole body
- no fading by pressure with glass tumbler - "tumbler test"
- resulting in purple bruising of skin
- photophobia
- headache, neck stiffness, vomiting
- irritability and/or confusion
vaccine
development history
- 1960s - purified PS vaccines for A and C
- immunity short term due to lack of T-cell involvement
- 1990s - conjugated vaccines for A and C after success of Hib conjugate vaccine
- 2000s - monovalent A vaccine for Africa
- "MenAfriVac"
current vaccines
- men C conjugate
- A,C,Y,W135
issues of men B vaccine
- polysaccharide of B is relatively low immunogenic
- the reason
- polysaccharide of B has potential toxicity for infant brain
- PS of B shows interaction with fatal brain cells which suggests potential of causing neurological damage for young infants